research proposal sample for phd in pharmacy

How to prepare a proposal for pharmacy research

A research proposal is often necessary to secure the required funding or resources. Cathy Geeson explains what to consider when putting a proposal together.

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When writing a research proposal you are aiming to produce a concise, clear summary of a proposed research project. This may form part of your academic studies, but often it is written to obtain the funding or resources needed to undertake the research. The proposal will need to be tailored to your audience, who may be academic supervisors, an organisation or an external funding body, but many of the principles of writing a research proposal remain consistent.

Putting together a proposal can take a considerable amount of time (an average of 9–12 months), so you need to be able to justify investing your time and that of your research team. You should approach writing a research proposal in the same way you would tackle any important project — do your background preparation, get the right team around you, make a plan and, finally, maintain your enthusiasm and determination to succeed.

The research topic

The most important thing to consider when choosing a topic is whether it poses a worthwhile question that needs to be answered and will result in tangible benefits within a reasonable and defined period. You should be able to demonstrate that the project will fill a gap in current literature.

Ask your peers and employers whether they believe the topic is important. Additionally, you could speak to the research team at the Royal Pharmaceutical Society (RPS) and members of the public to get their opinions.

Early considerations

Think carefully about what you want to achieve, whether funding is required and, if so, what type of funding may be suitable. Initially, you will need to consider how much money you are looking for and whether you are seeking a personal award, leading to a Masters or doctoral qualification, or funding for a larger research team. If the latter, you will need to demonstrate that you have enough experience to apply as the lead applicant.

You need to ensure that your proposal is practical and deliverable. Most awards are time-limited, typically between one and five years with most limited to three years, which means you will need to be realistic about how long you believe your research will take. Additionally, most awards are for a set amount of money, so you need to ensure that this is likely to cover all necessary resources and costs.

Different funding bodies will back different types of research so you will need to apply to the most appropriate organisation. For example, in the UK, the Medical Research Council funds basic or invention research whereas the National Institute for Health Research (NIHR) focuses on applied, evaluative and clinical research.

Ensure that the right infrastructure is in place within your organisation – this includes having appropriate management and support arrangements. Additionally, depending on the type of research, you may need to have access to sufficient patients and quality data. This may mean collecting your own data rather than trying to retrospectively assemble data that was not originally intended for research purposes.

Finally, you must be able to justify that your proposal is ethically acceptable. Although this does not mean preparing for ethics approval in detail at this stage, you should think about whether the benefits of undertaking the research outweigh the risks and burdens to potential participants.

Getting the right support

Your most important resource will be your research team. The members of your team will depend on your experience — for example, you may need an academic supervisor if the award is to support Masters or doctoral studies — and your research question and design; for example, you may require a statistician or a health economist. Decide who you require and try to obtain their support at an early stage. Be mindful of practical issues, such as the feasibility of arranging meetings. Support from your employer (and potential research site) is also crucial, particularly if you propose undertaking a secondment from your current role. At this stage you may also need to consider involvement from patients or the public or both (see ‘Patient and public involvement’).

It is also advisable to contact the research manager within your organisation and, depending on the research funder, you may also have access to design support. For example, the NIHR has a dedicated ‘research design service’ (RDS) to provide further guidance on the application process itself. The RDS also provides a number of training courses, together with ‘bid development’ advice, which can be valuable in helping hone your research proposal.

Try not to overlook other potential sources of help and advice. Researchers who have published work in the field may be willing to provide further advice on their methodology. My tip would be to seek as much advice and guidance as possible from a wide range of sources.

Once you have finalised your research methodology you can consider in depth what physical resources you will need, including access to patients, healthcare professionals and laboratory testing. The methodology will also inform the potential size and overall costs of your study. Talk to your finance department as early as you can — this can help ensure that your costs are thorough and realistic.

Writing your proposal

Research funding applications are generally highly structured and are split into sections that will vary by funder and funding stream. Each section will include clear instructions, usually including strict word limits. The funder is also likely to provide comprehensive guidance notes, plus an advice service should you need further clarification.

Remember that your proposal may be reviewed by panel members who do not work in your field, so avoid jargon and explain all abbreviations in full, ideally in each section (in case reviewers do not read your application in the order it was written). In terms of your writing style, aim for professional, clear and concise. Pay attention to detail, ask your research team to review your proposal and accept all offers to proofread your work.

Example of sections within the application form

Patient and public involvement (ppi).

Many funders are committed to the involvement of patients and the public so you may need to consider relevant activities as part of your application. These activities can involve patients and the public helping choose the research topic, assisting in the design, advising on the research project or actually helping carry out the research.

Plain English summary

You may be required to provide a brief summary of your research, written in language that members of the public should understand, so it is worth getting this reviewed as part of your PPI.

Scientific abstract

The scientific abstract is a more detailed summary that outlines the background to the research, the aims of the work, the plan of investigation and a synopsis of the potential benefits.

Background and rationale

You will then need to state your main hypothesis and research questions, and justify why the research is important and relevant to the funder. Think carefully about the benefits of your work — you will need to show the funder that your proposal is worth their investment. This section may also include your literature review, with details of gaps in current understanding of your topic, and how existing literature has informed your methodology. The funder will need evidence that you have carried out a thorough review, including any databases or citation indexes you have searched.

Research plan

In the research plan you should provide a structured protocol. It needs to be detailed enough to explain clearly how you intend to conduct the research but also succinct, because the word count is likely to be limited. You may also need to submit a ‘research timetable’ to highlight expected important milestones.

Expected outputs and dissemination

Additionally, you will need to assure the funder that the results of your research will deliver tangible benefits and that you will share these results widely.

Management and governance

You should be able to demonstrate that you will manage the award well, emphasising the results that you will deliver and how you will control the finances. This section may also include a review of ethical issues. Ensure that you are familiar with the ‘Research governance framework for health and social care’ from the Department of Health (England) and its implications for your work. Depending on the research methodology you may need to consider whether you will need informed consent from patients and other participants, and you will almost certainly have to address any confidentiality issues.

Intellectual property

Intellectual property (IP) provides the basis for protecting information, ideas and developments that your research may generate. The IP you generate will be retained by you and your organisation, but the funder will want to know that the IP will be protected (for example, with copyright or a patent) and used appropriately to ensure that the proposed research benefits can be delivered. Financial returns are an uncommon benefit of applied or clinical research but, where income generation is anticipated, you may need to enter into a commercialisation agreement with the funder to clarify how the revenue will be shared. This is an area where you may need to seek expert advice (for example, from ‘ NHS Innovation Hubs ’ ).

Making your proposal stand out

• Read the funder’s guidance notes carefully, and address each point thoroughly;
• Explain why yours is an important research question, with clear benefits;
• Be precise and succinct — could you describe clearly the main objective of your research in one or two sentences?
• Demonstrate that your proposal is well planned, feasible, cost-effective, and will yield high quality results with a positive impact;
• Justify everything fully, including your method, required resources and team members;
• Be consistent. For example, if you have said you need a PPI steering group, ensure this is included as a research cost and that meetings are built into your research timetable.

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Research Proposal Example/Sample

Detailed Walkthrough + Free Proposal Template

If you’re getting started crafting your research proposal and are looking for a few examples of research proposals , you’ve come to the right place.

In this video, we walk you through two successful (approved) research proposals , one for a Master’s-level project, and one for a PhD-level dissertation. We also start off by unpacking our free research proposal template and discussing the four core sections of a research proposal, so that you have a clear understanding of the basics before diving into the actual proposals.

• Research proposal example/sample – Master’s-level (PDF/Word)
• Research proposal example/sample – PhD-level (PDF/Word)
• Proposal template (Fully editable) 

If you’re working on a research proposal for a dissertation or thesis, you may also find the following useful:

• Research Proposal Bootcamp : Learn how to write a research proposal as efficiently and effectively as possible
• 1:1 Proposal Coaching : Get hands-on help with your research proposal

PS – If you’re working on a dissertation, be sure to also check out our collection of dissertation and thesis examples here .

FAQ: Research Proposal Example

Research proposal example: frequently asked questions, are the sample proposals real.

Yes. The proposals are real and were approved by the respective universities.

Can I copy one of these proposals for my own research?

As we discuss in the video, every research proposal will be slightly different, depending on the university’s unique requirements, as well as the nature of the research itself. Therefore, you’ll need to tailor your research proposal to suit your specific context.

You can learn more about the basics of writing a research proposal here .

How do I get the research proposal template?

You can access our free proposal template here .

Is the proposal template really free?

Yes. There is no cost for the proposal template and you are free to use it as a foundation for your research proposal.

Where can I learn more about proposal writing?

For self-directed learners, our Research Proposal Bootcamp is a great starting point.

For students that want hands-on guidance, our private coaching service is recommended.

Psst… there’s more!

This post is an extract from our bestselling short course, Research Proposal Bootcamp . If you want to work smart, you don't want to miss this .

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Thesis proposal

In Pharmacy, the MSc thesis proposal and the PhD thesis proposal are required courses (PHARM 601 and PHARM 616A/B, respectively). The objective is for students to learn how to use the literature to stimulate in-depth thinking about the basis of their thesis research project and to encourage the development of their scientific oral presentation skills, to best prepare and present their research objectives in written and oral form.

In addition to preparing a written and oral presentation of their proposed research, students must complete the following course requirements:

• Involves completing online modules as well as participation in an in-person session co-hosted by the Pharmacy Liaison Librarian and an Advisor from the Writing and Communication Center.
• Provides background on literature searching, citation and proper management of references as part of the preparation of the thesis proposal.  
• The workshop is offered once per term, as needed. 
• Students should attend in their first term, before they register in the thesis proposal course
• Workshop dates are communicated via email and/or Outlook calendar invitation.
• Attend a one-on-one appointment with the Pharmacy Liaison Librarian to discuss. research strategies and reinforce academic integrity.
• Attend two thesis proposals (or one thesis proposal and one thesis defence) by other students in Pharmacy, before their own thesis proposal examination.
• MSc students must hold the thesis proposal examination before the end of their second term.
• PhD students must hold their thesis proposal examination within their first year of the PhD program, before the end of term three.
• Any student requiring more time must request an extension, subject to the approval of the Graduate Officer.

The advisory committee appointment must be approved and the first meeting of the committee held before the proposal examination can take place.

Thesis proposal guidelines

The thesis proposal should outline the reasons for undertaking the project, concisely survey the relevant literature, present a detailed description of the methodology to be used, and outline any preliminary results.

Generally, a report of 30-40 pages is required, not including figures, legends, or references. Excess pages may be removed or disregarded.

Additional material including raw data may be included in appendices if there is a need for it to be included.

The completed thesis proposal should be double-spaced with 1-inch margins and size 12 font.  

The style of the report should follow conventions familiar to the area of research of the student.  At minimum, the written thesis proposal report should include the components indicated in the following table.

Students may wish to follow the  preparation of the thesis organization and formatting requirements, set by the Graduate Studies Office, to help prepare them for the final thesis submission.

Scheduling the thesis proposal examination

Follow the steps below when you are ready for your proposal examination:  

• Select two possible dates and times and ask your committee to save those dates until the exam is confirmed.
• Refer to "what to expect at the thesis proposal" to determine how much time you should book for your proposal (two hours is generally enough time for an examining committee with three examiners; additional time may be required for deliberation).
• If you did not sign up for the appropriate course (Pharm 601 or Pharm 616A/B) during the course enrolment period, complete and submit the Graduate Studies course drop/add form at the same time as submitting the meeting request form. 
• The grad coordinator will arrange the examination chair, prepare the proposal examination report, and set up IT support for the day of your exam (for in person and hybrid exams only).
• This is to ensure IT has the equipment/adapters necessary for the exam and not scrambling on the day of your exam.
• It will take approximately 15-30 minutes to go over everything.
• Your email request should be sent no sooner than one week prior to the test/training date.
• Submit an electronic copy of the (written) thesis proposal to each member of the examination committee and cc the grad coordinator at least 10 business days ahead of the proposal examination date.

What to expect at the thesis proposal examination

The oral examination will take approximately 2 hours and should consist of a 25-30 minute PowerPoint presentation, followed by questions from the examination committee.  Due to time limitations for the oral examination, it may not be possible to cover all aspects of the proposal in the presentation.

The question period will involve a first round of questions from the committee lasting 10-15 minutes per committee member, followed by a second round of questions in the same format but usually only 5-10 minutes each. Questions may be taken from the audience and the student's response to questions from the audience may be considered in the evaluation of the student. 

Thesis proposal examinations are not ‘public’ in the same sense that thesis defences are and are not announced throughout the Faculty of Science.  The administrative coordinator will inform pharmacy graduate students of upcoming proposal presentations so they may attend toward fulfillment of the thesis proposal course requirements.  External friends and relatives are not permitted to attend. 

Following the oral examination, the audience and students are excused so the committee can deliberate. All examiners should be present for deliberation.  After deliberation, the student is invited back into the room to hear the results of their exam. Students will receive a summary of their final grading assessment once the report has received approval. 

Assessment of the thesis proposal

Assessment of the thesis proposal is twofold:  The written proposal report and the oral presentation and discussion are each marked separately and independently by three or more committee members (the examining committee) using the thesis proposal grading sheet, following the grading scheme below. The final course grade is calculated by averaging the total scores of all examining committee members; t he assessment of whether or not the student has met the standards for the proposal and for progress in their graduate program overall, is recorded on the thesis proposal examination report . All members of the thesis proposal examination committee participate in grading and in the assessment of the student's overall progress.

Thesis proposal grading scheme

Students must complete all graduate courses with a final mark of 70% or greater, as noted in the Academic Calendar.

Thesis proposal examination report

The decision as to whether standards for the proposal and progress to date are met is made by the committee, recorded by the chair, and reported to the Faculty of Science usingthesis proposal examination report. Committee members assesses the student's position by indicating 'excellent', 'satisfactory', or 'unsatisfactory', in the following areas:

• Understanding of the material: Candidate shows adequate depth and scope of knowledge for the current stage of the project;
• Ability to handle discussion: Candidate is able to understand the pitfalls and interpretation of the project;
• Research progress: Student demonstrates a general level of progress considering the complexity of the work and practical difficulties.

Performance and standards of research concerning expectations for the degree level as well as they pertain to timely completion of the degree are indicated with a yes/no response.  Any questions, concerns, difficulties or corrective measures required by the student must be recorded in the comments sections of the report; the committee must specify an action plan outlining what the student is expected to do by a specified date. 

Pharmacy blackout dates

Pharmacy has blackout dates during which thesis proposals and PhD comprehensive exams are not be held unless special arrangements have been made and confirmed in advance by the pharmacy graduate office. Blackout dates exist to allow maximum participation in the Pharmacy program and to minimize scheduling conflicts for examination chairs and committee members. 

Blackout dates are also noted on the Pharmacy Graduate Studies Outlook calendar. 

• Thesis formatting
• Thesis information
• Academic Calendar - School of Pharmacy

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PhD in Pharmaceutical Outcomes Research

Pharmaceutical Outcomes Research is a PhD program in the graduate program in Clinical Pharmacy. This program is housed in the Center for Pharmaceutical Outcomes Research (CePOR, SEE-por), a school-wide center in the Skaggs School of Pharmacy. Our doctoral curriculum is designed to provide competent and highly skilled researchers in the study of patient, provider, or population-level health care and health system interventions. We most often focus on economic, clinical, and humanistic outcomes such as clinical or cost effectiveness or safety. Areas of focus available to students undertaking this course of study include pharmacoeconomics, pharmacoepidemiology, health services research, and drug policy.​​​

Core faculty are methodological experts and provide collaborative linkage to clinical experts in all pharmacy, medicine, nursing, and public health. Programs of study are tailored to student interests in disease or drug areas, such as cardiology, psychiatry, neurology, and cancer. Opportunities exist to link to more basic science colleagues depending on your topic of interests. For example, students interested in drug safety might link with toxicology faculty, or in gene-environment interactions might link with pharmacogenomics faculty.

Applications for all doctoral programs are submitted electronically through the Graduate School of the University of Colorado Denver. After signing up for an account, select 'PhD' under the 'Academic Interests' menu and scroll down to 'Skaggs School of Pharmacy and Pharmaceutical Sciences' and select "PhD in Pharmaceutical Outcomes Research."

Application requirements are:

• A completed Graduate School application and $50.00 application fee (Domestic) $75.00 application fee (International)
• A baccalaureate degree of arts or science from an accredited college or university with a minimum GPA of 3.0.** One (1) official transcript of all academic work completed to date with awarded baccalaureate degree. University transcripts from other countries must include a transcript evaluation from World Education Services ( WES ). Applicants who complete a transcript evaluation with WES will have their application fee waived automatically.
• All applicants for the program should complete a year of study in the following subjects: general chemistry, organic chemistry, calculus, biology, English and physics. In addition, courses in the following subjects are highly recommended to supplement the student's background: physiology, biochemistry, statistics, cell biology, physical chemistry, and computer science.
• Three (3) letters of recommendation from professors or research supervisors familiar with your aptitude for graduate study

Additionally:

• The GRE (Graduate Record Examination) is not required but is optional.
• The TOEFL is required of applicants for whom English is not their first language, Duolingo and IELTS also accepted (more information on this  here )
• Please use 4875 as the Institution Code so that the test results will be sent directly to our institution
• Under special circumstances, deficiencies in important areas may be made up within the first year after entrance into the program. Normally, admission to the program will be based on an undergraduate GPA of 3.0 or better. However, applicants' recommendations, research experience and additional individual accomplishments will also be considered in the admissions process.

Application opens September 1, 2023. Applications will not be reviewed until all required materials have been received. The application deadline for Fall 2024 admission is December 1, 2023 for all students.

Admission to the program may include financial support via a stipend awarded on a 12-month basis.

Although a priority of the School of Pharmacy is to provide financial support to its graduate students, payment of stipend, tuition and any fees by the School of Pharmacy or by grants, contracts or gifts to the School of Pharmacy faculty is contingent upon availability of funding, satisfactory academic progress (as defined by the UCD Graduate School, Graduate Student Handbook) and completion of required teaching duties, core courses, and examinations. The School of Pharmacy also reserves the right to review and adjust its funding policies at any time. All students are expected to work full-time toward program requirements for 12 months of the year.

Generally, the first year of financial support will be in the form of stipend support for working as a teaching assistant. Depending on availability, teaching assistantships may be offered beyond one year to students. Faculty may choose to offer research assistant scholarships to students as well. Other funding opportunities in the form of external student grants and awards also exist. Students are encouraged to talk to the faculty about funding and scholarship opportunities. Funds for travel to one meeting where students are presenting a poster or giving a podium presentation are limited to $500 per fiscal year.

Students who do not remain in good graduate standing (3.0 GPA or above) or maintain satisfactory academic progress are placed on academic probation. Probation and suspension policies are described in the UCD Graduate School, Graduate Student Handbook. Payment of stipend, tuition, insurance and fees for a student while on academic probation is at the discretion of the graduate program committee.​​

What does "pharmaceutical outcomes research" mean?

What kind of students should pursue a phd degree in pharmaceutical outcomes research why should you apply to this program.

We are looking for students who want to influence healthcare but do not want to be a provider. With the belief that the research done will allow for the application of new knowledge towards health improvement.

What makes the Pharmaceutical Outcomes Research PhD program at the University of Colorado different from other PhD programs?

The benefits of this program are multi-faceted. Housed on a major medical campus, students will be able to collaborate with the schools of pharmacy, medicine, nursing, and public health. Also the University of Colorado Hospital, Children's Hospital, and the Veterans Affairs Medical Center are located on campus.

By having a small group of graduate students, they are allowed more time with the faculty members. With two faculty members from each component, students will be able to have the support necessary to complete their degree.

What are the job prospects for a graduate with a PhD degree in the pharmaceutical sciences? What can you do with this career?

Graduates of the program will have many career options within these areas:

• Pharmaceutical industry
• Government agencies
• Contract research organization (CROs)
• Organized healthcare systems

There is a critical need for individuals who are able to conduct rigorous, credible, and relevant population and patient-based research within stringent ethical and regulatory guidelines; the demand for such researchers is expected to grow given the developing health care reform and the investment in federal development and expansion on comparative effectiveness research.

Past graduates have gone on to be an interim dean at a Regis University and the director of pharmacy at the University of Colorado Hospital

How are current students doing?

Our students often win awards at regional and national symposium (such as Julia Slejko at ISPOR or SMDM). One holds a prestigious pre-doctoral dissertation award in health outcomes from the PhRMA Foundation. Two have completed comprehensive exams are working on defending their dissertation proposals. All these more advanced students have published manuscripts in peer-reviewed journals as first authors with the mentorship of the CePOR faculty.

Faculty comments on the program.

Heather Anderson, PhD What's great about this campus is that we are able to collaborate with other schools such as public health, nursing, and medicine. While many Pharmaceutical Outcomes Research programs have a major focus on economics, we do that and more. Our program has a strong focus on epidemiology and policy too. I actually got my PhD in epidemiology from our School of Public health and can link up students with the best courses and advise on exciting local opportunities for research assistantships.

Kelly Anderson, PhD Training at a world-class medical campus allows PhD students in the Center for Pharmaceutical Outcomes Research to engage with faculty in the center with expertise in outcomes research, drug pricing, economics, epidemiology, and health policy, and also have the opportunity to learn from and collaborate with faculty throughout the Schools of Pharmacy, Public Health, Medicine, Dentistry, and Nursing. For anyone who loves big data, our faculty also work with numerous large data sets: Medicare claims, linked EHR-claims data, and all-payer data just to name a few. As a lot of my work is focused on payment policy, I welcome the opportunity to engage students as they think about the real-world implications of their research for policy makers, health insurers, patients, clinicians, and drug companies and disseminate their findings to these key stakeholders.

R. Brett McQueen, PhD Pharmaceutical outcomes research includes aspects of multiple disciplines including math, economics, and epidemiology. I joined the faculty at CU to contribute to comparative- and cost-effectiveness research and to education both for the PhD and the PharmD programs. Our PhD program emphasizes quality over quantity. We maintain a very favorable student to faculty ratio, we offer competitive student financial support, and we strive to graduate scientific leaders in the field of outcomes research.

Kavita V. Nair, PhD Our expectations for graduate students are high and we have structured the education and training requirements to help you meet these goals. I will require a lot of you as a student but will also be your strongest advocate!

Robert Valuck, PhD, RPh I believe that the strengths of our program are the skills and the diversity of the faculty, and size and connectedness of our program with others on campus and in the state and region. With a smaller number of graduate students in our program, they are able to spend more time with faculty members. Our program is well connected with others on the Anschutz campus, and students have opportunities to collaborate both across campus, and with state agencies, provider groups, and others that have an interest in outcomes research and its applications to patient care and policy.

Advance the science of pharmaceutical outcomes research by training scientists who generate and synthesize evidence to inform practice and policy.

The goal of the PhD n pharmaceutical outcomes research is to develop methodological experts. Graduates will have the knowledge and extensive skills necessary to conduct pharmacoeconomic, pharmacoepidemiologic, health services, and drug policy research. We train individuals who can contribute to T3-T4 clinical translational pharmacy and pharmaceutical sciences, specifically on effective, population health, and policy studies. These contributions should ultimately benefit pharmacists and society with safe, effective, and efficient use of pharmaceutical care.​​

The Pharmaceutical Outcomes Research PhD program trains graduate students to become proficient and successful investigators who are able to:

• demonstrate an in-depth knowledge of central concepts in Pharmaceutical Outcomes Research, including the areas of pharmacoeconomics, pharmacoepidemiology, and/or drug policy.
• critically appraise existing literature and sources of information.
• formulate hypotheses based on current concepts in the field and accurately and correctly design, conduct, and interpret their own research projects.
• present research results in peer-reviewed publications and in a dissertation.
• perform research that adheres to the principles and guidelines of ethical conduct.
• communicate research results effectively through oral presentations at scientific seminars, conferences, and other venues

The program’s strengths in outcomes research are emphasized in 35 credits of several areas:

• Biostatistics
• Epidemiology
• Health Policy
• Research/Study Design
• Doctoral Thesis

The program has experience in accessing a multitude of data such as MEPS, PHARMetrics, University Health-System, Consortium and MarketScan. Students are encouraged to utilize these datasets as well as primary data collection. Students may enroll in courses not listed (e.g courses in downtown campuses and/or newly developed courses) by consulting with the program director.

Pharmacoepidemiology

Heather Anderson PhD

Robert Valuck PhD, RPh

Pharmacoeconomics.

Mike J. DiStefano PhD, MBE

Kelly Anderson PhD, MPP

R. Brett McQueen PhD

Pharmaceutical and drug related policy.

Kavita Nair PhD

Antal Zemplényi

Antal Zemplényi, PhD, is an Associate Professor at the Center for Health Technology Assessment at the University of Pécs and a senior researcher at the Syreon Research Institute, an international research corporation specializing in health policy, health economic modeling, and technology assessment. He has experience in value assessment, HTA, health economics and outcomes research, and real-world data analysis. He is the past president of the ISPOR Hungary Chapter. Antal is currently a Fulbright Scholar at the University of Colorado Skaggs School of Pharmacy and Pharmaceutical Sciences working as a visiting research associate in the Pharmaceutical Value (pValue) initiative.

Monica Bianchini

Monica Bianchini is originally from Indianapolis, Indiana. She received a PharmD and MPH from the University of Wisconsin-Madison in 2017. She subsequently completed a hospital pharmacy residency (PGY-1) and Infectious Diseases PGY-2 at Henry Ford Hospital in Detroit, Michigan. Monica joined CePOR in 2019 and currently works as a clinical inpatient pharmacist. Her dissertation will evaluate opportunities to decrease syphilis rates and improve syphilis care in Colorado. Outside of work, she enjoys reading, live music, cooking, and anything outside (running, hiking, backpacking, skiing). 

Sue is a fifth year PhD student at CePOR. Her dissertation focuses on characterizing the burden of MS and treatment strategies using real-world claims data. Prior to grad school, she studied Neuroscience in Pomona College. In her free time, Sue enjoys taking her puppies on adventures.

Mahesh Maiyani

Mahesh Maiyani was born and raised in India. He earned his Bachelor of Pharmacy (BPharm) from India in 2006 and then he came to the US to pursue his Master’s in Business administration. He completed his MBA from The University of Findlay in Ohio. He has work experience in clinical trials and heath care research. He joined the Pharmaceutical Outcomes Research PhD program in Fall-2021. His research interests are focused around cost effectiveness in real-world clinical settings. Mahesh enjoys hiking and spending time with family and friends.

Nick Mendola

Nick Mendola was born and raised in Buffalo, New York. He graduated from The University of Akron with a BS in Exercise Science in 2016. He then moved to Washington D.C. to attend The George Washington University Milken Institute School of Public Health, where he obtained his MPH in Epidemiology, in 2018. During this time, he worked researching the impact of the pharmaceutical industry’s marketing to healthcare professionals, and its influence on prescribing practices and population level drug utilization. Nick joined the Pharmaceutical Outcomes Research program in the fall of 2018. Nick’s current work with Dr. Robert Brett McQueen, explores the use of Multi-Criteria Decision Analysis (MCDA) as a novel health technology value assessment tool. His work specifically explores MCDA in evaluating treatments for neuromyelitis optica spectrum disorder (NMOSD), a rare neurological disorder.

Vanessa Paul Patterson

Vanessa Patterson is originally from Kansas City. She graduated from Tulane University School of Public Health and Tropical Medicine with an MPH concentrating in Epidemiology and Maternal and Child Health in 2012. Vanessa went on to work as an applied epidemiologist for government public health agencies for six years. She joined the Pharmaceutical Outcomes Research program at CU in the fall of 2018. Working under the mentorship of Dr. Heather Anderson, Vanessa is currently a PhRMA Foundation Predoctoral Fellow and a PhD candidate. Her dissertation focuses on the utilization of cardioprotective medications among women with a history of breast cancer. In her free time, Vanessa enjoys making pottery and spending time outdoors with family and friends.

Nai-Chia (Sammi) Chen

Sammi is originally from Taiwan. She holds a bachelor’s degree in Pharmacy from Kaohsiung Medical University. After graduation, she had worked in pharmaceutical companies and clinical research organizations for several years before coming to the US. She completed her Master’s training at the University of Pittsburgh, Pharmaceutical Outcomes and Policy Research, in 2022. And then she joined Pharmaceutical Outcomes Research PhD program at CU Anschutz in Fall 2022. Her research interest lies in the intersection of pharmacoeconomics, real-world evidence, and pharmaceutical outcomes. Outside the schoolwork, she enjoys cooking, baking, and snowboarding/skiing in winter.

Mouna Dardouri

Mouna was born and raised in Tunisia. She graduated with a PharmD from the University of Pharmacy of Monastir in 2016. She then worked for two years at a consulting company focusing on pharmaceuticals’ Pricing, Reimbursement and Market Access (PRMA) in Europe. After that, she was awarded with the Fulbright Foreign student scholarship and moved to Colorado, where she obtained her MPH in Global Health Systems, management, and Policy in 2022. Mouna joined the Pharmaceutical Outcomes Research program in the fall of 2022. Her research interests include evaluating the use of Health Technology Assessment in the context of low- and middle- income countries and developing tools that permit equitable patients’ access to cost-effective technologies. In her free time, Mouna enjoys learning new languages, improv theatre and cooking. 

Why CU's Pharmaceutical Outcomes Research PhD Program?

“One key reason I chose to join CePOR at CU was the tight-knit group of faculty and students. Given the program is smaller, the faculty has a better opportunity to stay in touch with all the students and provide support for everyone's research, regardless if they're on the student's committee or not. The student group is also very close as we are together for weekly seminars and enjoy out-of-school gatherings when possible. Another draw of CU's POR program is the diverse expertise of our faculty and alumni. Our current faculty have a range of expertise including: pharmacoepidemiology using big data sources, pharmacoeconomics and drug pricing, rare diseases, opioid use disorder and treatment, and Medicare payment models. Recent alumni have found work in a variety of different fields from consulting to academia to the pharmaceutical industry and the public health department. The wide range of backgrounds and areas of expertise covered by our faculty and alumni provide so many resources for mentorship and future career planning. Finally, there are so many unique opportunities within CePOR to work with different data sources (e.g. electronic health records, national claims data, Medicaid claims data) and different methodology experts, so I am confident that our program could be a great fit for prospective PhD students of all backgrounds.” – Monica Bianchini, PharmD, MPH

“CU's Pharmaceutical Outcomes Research Program produces robust interdisciplinary research that spans from pharmacoepidemiology to pharmaceutical economics with a variety of collaborators, such as Institute for Clinical and Economic Review (ICER) and Colorado Department of Public Health & Environment (CDPHE).” – Sue Kwon, BA

“I joined the POR program because my previous research was focused on population drug utilization and the pharmaceutical industry’s impact on prescribing practices, and the POR program seemed like a natural fit for me to be able to keep learning about the areas of pharmacoepidemiology and drug related policy. What I like most about the program so far has been the core faculty in our program. They seem to truly care about student success and how we progress both academically and professionally. ” – Nick Mendola, MPH 

PhD Student Research Projects

• Comparative Effectiveness of Rare Disease Therapies Using Multi-Criteria Decision Analysis: Case Example in Neuromyelitis Optica Spectrum Disorder, a Rare Neurological Disorder
• Characterizing Real-world Burden of Multiple Sclerosis and Treatment Strategies in a Colorado-representative Population
• Utilization of Cardioprotective Medication Strategies Among Women with a History of Breast Cancer
• Opportunities to Improve Syphilis Care in Colorado

Mission: To educate, increase awareness and promote growth within the 'Pharmacoeconomics and Outcomes Research' field in general and to increase the CU Denver presence among the international society ISPOR. To collaborate across different sciences on campus and different departments worldwide.

Description: Promote pharmacoeconomics and outcomes research education by holding regular seminars on current issues in the field and presenting research at least once a year at the annual meeting in the US-Canada region.

Membership requirements: We expect members to be passionate about the kind of research that is involved related to public health, epidemiology, pharmacoeconomics, and policy. Also, attending our regular educational seminars/webinars is highly encouraged.

Activities: Details will be emailed to members soon!

Benefits: The opportunity to present research, network and collaborate with faculty from different universities around the world, professionals from industry and research organizations at a global level.

Julia Slejko, PhD ('12) Associate Professor Practice, Sciences, and Health Outcomes Research University of Maryland School of Pharmacy

R. Brett McQueen, PhD ('13) Associate Professor Department of Clinical Pharmacy, Skaggs School of Pharmacy and Pharmaceutical Sciences University of Colorado Anschutz Medical Campus

William Padula, PhD ('13) Assistant Professor of Pharmaceutical and Health Economics, School of Pharmacy Fellow, Leonard D. Schaeffer Center for Health Policy & Economics University of Southern California

David Tabano, PhD ('18) Principal Health Economist Evidence for Access (E4A) | Public Affairs & Access Genentech, Inc.

Katie Sullivan, PhD ('18) Prescription Drug Epidemiologist Colorado Department of Public Health and Environment

Angela Czaja, MD, PhD ('19) Associate Professor Pediatrics-Critical Care Medicine Children’s Hospital Colorado Anschutz Medical Campus

Chong Kim, PhD ('20) Associate Director Global Value & Access | HEOR Gilead Sciences

Katia Hannah, PhD ('21) Lead HEOR Specialist Dexcom

Kimberly Deininger, PhD ('22) HEOR Manager Amgen

For questions regarding graduate school programs contact:

Isabella Jaramillo Email:  [email protected]     Phone:  303.724.7263 ​​​​​

Kelly Anderson, PHD, MPP

Assistant Professor; Director, Pharmaceutical Outcomes Research PhD Program Email: [email protected] Phone: 434-466-1990

CU Anschutz

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Aurora, CO 80045

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Research Proposal Guidelines

To satisfy the research requirement for the distance M.S. program in Pharmaceutical Chemistry, the aspiring student must define a research project and prepare a written proposal describing the nature and goals of the project.

It is suggested that the student in conjunction with their distance research mentor collaborate in the selection of and the definition of the proposed research. The proposal should consist of the following elements:

• Overall goal or hypotheses
• Statement of significance of the research
• Research plan consisting of several specific aims.

The following description serves to define expectations regarding proposal preparation.

Project Title

An appropriate title should be created that describes the overall research topic.

Overall Goal

Write a short statement that clearly defines the scope of the project.

Background and Significance

Become familiar with a published work that is related to your chosen research area. Provide a summary of the background in a manner that demonstrates a knowledge of the area and goes on to describe the significance of the proposed research in adding to and extending existing knowledge.

Specific Aims

The overall project should be envisioned as a series of sub-goals, which as they are individually accomplished, allows results in the achievement of the overall goal.  The specific aims should include a description of the experiments to be conducted. It should be clearly stated what is to be accomplished in each specific aim and how these results relate to the achievement of the overall research goal.

Bibliography

Appropriate literature citations should be provided in each section of the proposal, as justification for the proposed research, and to clearly indicate that the student has familiarized themselves with the research topic.

The M.S. research proposal should be limited to approximately four pages, excluding the bibliographic section.

The proposal preparation will satisfy one credit hour of the research requirement.

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A Practical Guide in Writing a Medicinal Chemistry Research Proposal for Students Entering Research

The aim is to give an overview summary of the research and discuss the merits and broader impacts of the research project. The quality of the research proposal depends not only on the quality of the research you proposed but also included the writing of your project. Research proposal help assist students in a different way to fulfill their academic goals. Some students that have lack of subject knowledge feel it challenging to feed the readers with sufficient information in the proposal, so there is a consultation PhD proposal writing service with the expert help supply all the central details on the project. The role of new researchers while writing a medical chemistry research proposal is to make the readers that the solution for the research question is practical and appropriate. Students find it challenging to write a quality PhD research proposal by considering the organization format. When you Order any reflective report at Tutors India, we promise you the following; Plagiarism free, Always on Time, Outstanding customer support, Written to Standard, Unlimited Revisions support, High-quality Subject Matter Experts. Contact: Website: www.tutorsindia.com Email: [email protected] United Kingdom: +44-1143520021 India: +91-4448137070 Whatsapp Number: +91-8754446690 Read more: https://bit.ly/32U6O8J

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Peer reviews became commonplace in most sciences only after the Second World War. For example, Albert Einstein's revolutionary papers in 1905, Annalen der Physik, were never peer-reviewed by anyone else than the journal's editor and co-editor: "in journals in those days, the burden of proof was generally on the opponents rather than the proponents of new ideas. The peer reviews usually side with the proponents of the old ideas and it is the responsibility for the new ideas to prove themselves right. The peer review of eclectic research that newly fuses two distant research disciplines is the most demanding and contentious of all types of peer reviews: one discipline may face a strong resistance from another especially if it requires an alteration to its long-cherished paradigms, long seen as fundamental idea in the other discipline. A genuine interbreeding of work into another research discipline increases a probability that the weaknesses in the original major paradigms are identified, exposed and improved. Many Nobel prizes have come this way.

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A book like this cannot be written in isolation. While most of the text found in this manual is original, dozens of similar books and experts were consulted, and many colleagues and friends provided information, feedback, and suggestions. My greatest thanks goes to Nancy Vyhmeister, author of the first AIIAS writing manual, for her willingness to share original content and ideas from her work. Chapter 1 is taken largely from her prior work. She was also instrumental as a consultant for the Turabian chapter and in overall editing of this book. Thanks also to Juanita Bissell, for contributing the basis for the Turabian chapter from her earlier AIIAS Turabian manual. This has been revised, updated, and shortened, but her work is still the basis for Chapter 6. Thanks to Elsie Dela Cruz, Prema Gaikwad, and Esther Papaioannou for their substantial contributions to the APA explanations in Chapter 7. Thanks also to Bonnie Proctor, the editor at Andrews University, for her willingness to share ideas, resources, and materials. By now it is difficult to tell where her ideas end and mine begin, but some of her work is included especially in the introduction, and in the chapters on academic writing conventions, mechanics, APA and Turabian. Her support has been much appreciated.

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Pharmacy Research Proposals Samples For Students

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• Potential Research Projects

Research projects for Higher Degree by Research (HDR) students are available within the following School of Pharmacy research areas and research centre. 

Please email our academic staff to discuss potential HDR projects and ask if they are available as an advisor for your proposed HDR program.

Clinical Pharmacy and Pharmacometrics

Title: Implementing Pharmacogenomics into Community Pharmacy Practice to Personalise the Treatment of Depression Contact:  Associate Professor Chris Freeman

Title:  Developing pharmacokinetic models for immunosuppressants in solid organ transplant patients Contact:   Dr Christine Staatz

Title:  Improving the use of immunosuppressant agents in solid organ transplant patients Contact:   Dr Christine Staatz

Medication Use, Safety and Health Services Research

Title:  The ethics of pharmacogenomic testing in community pharmacy Contact:  Doctor Adam La Caze

Title: Pharmacy ethics and the opioid crisis Contact:  Doctor Adam La Caze

Title:  Improving the use of immunosuppressant agents in solid organ transplant patients Contact:   Dr Christine Staatz

Title:  Establishing pharmacokinetic and pharmacodynamic models for antibiotics used in special paediatric populations Contact:   Dr Christine Staatz

Title:  Queensland Family Cohort (QFC) : Characterising medication usage within the perinatal-postnatal family environment Contact:   Dr Meng-Wong Taing

Title:  Pharmacy and oral healthcare Contact:   Dr Meng-Wong Taing

Pharmacoepidemiology, Pharmacovigilance and Pharmacoeconomics

No projects currently available.

Biotherapeutic Delivery and Diagnostic Solutions

Title: Computer-aided design, synthesis and evaluation of targeted drug delivery systems Contact:   Dr Ben Ross

Title:  Engineering peptides and proteins as therapeutics Contact:   Dr Peter Moyle

Title:  Improving the delivery characteristics of protein / peptide drugs Contact:   Dr Peter Moyle

Title:  Deciphering the roles of post-translational modifications Contact:   Dr Peter Moyle

Title:  Recombinant, semisynthetic and synthetic vaccines Contact:   Dr Peter Moyle

Title:  Targeted delivery systems for RNAi and DNA delivery Contact:   Dr Peter Moyle

Title:  Enhancing the activity of antimicrobial agents Contact:   Dr Peter Moyle

Title:  Engineering nanostructures and nanomedicines using supercritical fluid technology Contact:   Dr James Falconer

Title:  Improving delivery of challenging to formulate bioactives using advanced delivery systems Contact:   Dr James Falconer

Title:  Discovery of new drugs from indigenous Australian plants using supercritical fluids Contact:   Dr James Falconer

Title:  Design, construction, and development of supercritical fluid technology Contact:   Dr James Falconer

Title:  Characterisation of high pressure spray behaviour and bioactive Contact:   Dr James Falconer

Title:  Delivery of therapeutics to the posterior eye Contact:   Dr Harendra Parekh

Title:  Development of bioresponsive drug/gene carrier systems Contact:   Dr Harendra Parekh , Dr Karnaker Tupally

Title:  Bioresponsive porous silicon-polymer composite nano- and micro-particles for oral protein delivery Contact:   Dr Amirali Popat

Title:  Mesoproous silica nanoparticles synthesis and application in drug delivery, diagnosis and therapeutic protein delivery Contact:   Dr Amirali Popat

Title:  Inorganic nanoparticles for targeting bacterial biofilms Contact:   Dr Amirali Popat

Pharmaceutical Biology

Title:  Calcium homeostasis in cancer: identification and characterisation of novel drug targets  Contact:  Professor Greg Monteith  and  Professor Sarah Roberts-Thomson

Title:  Identification and characterization of novel ion and drug transporters and the design of novel high throughput screening assays for new pharmaceuticals Contact:   Professor Greg Monteith

Title:  Physiological regulation and the role of calcium transporters   Contact:   Professor Greg Monteith

Title:  Morphine and metastasis Contact:   Associate Professor Marie-Odile Parat

Title:  Role of caveolar proteins in glioblastoma Contact:   Associate Professor Marie-Odile Parat

Title:  Effect of perioperative pharmacotherapy of cancer patients on tumour Biology  Contact:   Associate Professor Marie-Odile Parat ,  Dr Ben Ross  and  Professor Nick Shaw

Biomedicinal Discovery and Development

Title:  Design, synthesis and evaluation of novel molecules for the treatment of Alzheimer's disease Contact:   Dr Ben Ross

Title:  Computer-aided design, synthesis and evaluation of new drugs for cancer, pain and neurodegenerative diseases Contact:   Dr Ben Ross

Pharmacy Education Research Centre

No current projects available.

Alan Grant-Taylor Memorial Scholarship: Community Pharmacy Practice

Find out more about the Alan Grant-Taylor Memorial Scholarship

UQ Summer and Winter Research Programs

Coordinated by the UQ Student Employability Centre, these programs provide an opportunity for scholars to work with a researcher in a formal research environment in their area of interest.

By participating in a program students will gain valuable academic and professional opportunities, develop analytical, critical thinking, and communication skills, and have an opportunity to cultivate links with industry and academic contacts. 

It is also a chance to ‘test drive’ research before embarking on further research studies or higher degree research projects. Participation is open to undergraduate students and Masters by coursework students.

All students participating in the summer and winter programs will receive a scholarship. General information on the program, including how to apply, is available from the UQ Student Employability Centre’s program website .

Please see our Summer and Winter Research Program page for a full list of the available programs.

• Research Areas
• Higher Degrees by Research
• Optimising Medicine Information Handover After Discharge (OPTMED-D)
• Safe and Effective Medication Collaborative
• Seminar Series

UKnowledge > College of Pharmacy > Theses & Dissertations

Theses and Dissertations--Pharmacy

Theses/dissertations from 2024 2024.

Design of Kappa Opioid Receptor Agonists for Potential Treatment of Multiple Sclerosis , Lindsay Kornberger

Theses/Dissertations from 2023 2023

Self-Assembled Ternary Polypeptide Nanoparticles With Improved Biostability For Drug Delivery In Cancer Therapy , Preye Mike Agbana

Investigation of Folate-Poly(Glutamic Acid)/Polyethylenimine/DNA Complexes for in vitro Gene Delivery , Caleb Akers

POPULATION-BASED EVALUATION OF TREATMENT PATTERNS, DRUG-DRUG INTERACTIONS, AND CARDIOVASCULAR RISK IN PATIENTS WITH METASTATIC CASTRATION-RESISTANT PROSTATE CANCER , Yue Cheng

An Epidemiological and Pharmacokinetic-pharmacodynamic Investigation into the Impact of Carbapenem-resistant Enterobacterales , Justin Clark

STRIVING FOR APPROPRIATE ANTIBIOTIC USE: A BIOMARKER INITIATIVE, AND OUTCOMES ASSOCIATED WITH AZITHROMYCIN EXPOSURE , Amanda Gusovsky

New Tools for Biocatalysis: Studies on the Carminomycin 4-O-Methyltransferase DnrK , Elnaz Jalali

Optimization of Orally Bioavailable Inhibitors of Defective in Cullin Neddylation 1 (DCN-1) , Leah Kovalic

Genetic and Pharmacogenetics Associations of Cancer Disparities in Appalachia , Nan Lin

Design and Synthesis of Small Molecular Inhibitors of DCN1-UBE2M Interaction , Tucker J. Moseley

Effectiveness of a long-acting cocaine hydrolase in metabolizing cocaine and its physiologically active metabolites , Linyue Shang

Anti-Inflammatory and Analgesic Effects of Highly Selective Microsomal Prostaglandin E2 Synthase-1 (mPGES-1) Inhibitors , Madeline Stewart

INVESTIGATING THE USE OF mPGES-1 INHIBITORS FOR THE TREATMENT OF ABDOMINAL AORTIC ANEURYSMS , Lauren M. Weaver

DEVELOPING A BIOCATALYTIC TOOLBOX TO AID IN UNDERSTANDING NUCLEOSIDE ANTIBIOTICS , Jasmine Brianna Woods

BIOINFORMATIC ANALYSIS OF PROTEOMIC AND GENOMIC DATA FROM NSCLC TUMORS ON PROGNOSTIC AND PREDICTIVE FACTORS OF IMMUNOTHERAPY TREATMENT , Mark Wuenschel

Theses/Dissertations from 2022 2022

Response of Dopaminergic System to Cocaine Exposure, Recovery after Cocaine Abstinence, and Impact of a Long-acting Cocaine Hydrolase , Jing Deng

ANALYSIS OF POTENTIAL FACILITATORS TO USE OF HIV PRE-EXPOSURE PROPHYLAXIS (PrEP) IN A YOUNG TRANSGENDER POPULATION , Noah Dixon

Studies Toward the Development of an Improved Countermeasure for Synthetic Opioid Overdose , Sidnee L. Hedrick

Development of zafirlukast derivatives active against Porphyromonas gingivalis , Kaitlind C. Howard

Investigating the Physical Stability of Amorphous Pharmaceutical Formulations , Travis W. Jarrells

THE RELATIVE CONTRIBUTION OF LIVER AND INTESTINE IN REVERSE CHOLESTEROL TRANSPORT , Rupinder Kaur

LIPOSOMAL TECHNOLOGIES TO IMPROVE GENE DELIVERY , David Nardo Padron

DEVELOPMENT OF ACCURATE AND EFFICIENT COMPUTATIONAL METHODOLOGIES FOR PREDICTING PROTEIN-LIGAND AND PROTEIN-PROTEIN BINDING FREE ENERGIES , Alexander Hamilton Williams

BUILDING TOOLS FOR IMPROVED MODULATION OF THE HUMAN GABAA RECEPTOR, A CENTRAL NERVOUS SYSTEM TARGET FOR THE TREATMENT OF ANXIETY , Garrett Edward Zinck

Theses/Dissertations from 2021 2021

UNDERSTANDING ABSORPTION, SUPERSATURATION, AND DRUG ACTIVITY IN SOLUTION: WORKING TOWARDS DEVELOPING A MORE BIORELEVANT MEDIA , Freddy Arce

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