clinical research associate salary in us

How much does a Clinical Research Associate make in the United States?

• Clinical Research Associate Salary The average Clinical Research Associate salary in the United States is $119,893 as of March 26, 2024. The range for our most popular Clinical Research Associate positions (listed below) typically falls between $58,136 and $181,651. Keep in mind that salary ranges can vary widely depending on many important factors, including position, education, certifications, additional skills, and the number of years you have spent in your profession. With more online, real-time compensation data than any other website, Salary.com helps you determine your exact pay target.
• Clinical Research Associate II Participates in the design, administration and monitoring of clinical trials. Analyzes and evaluates clinical data gathered during research. Ensures compliance with protocol and overall clinical objectives. Knowledge of FDA regulatory requirements is required. May require ACRP or SOCRA Clinical Research Professional exam completion. Requires a master's degree in science or equivalent. Typically reports to a supervisor or manager. Occasionally directed in several aspects of the work. Gaining exposure to some of the complex tasks within the job function. Typically requires 2-4 years of related experience. View Clinical Research Associate II Salary Alternate Job Titles :Clinical Trails Research Associate II, Clinical Trials Data Analyst II, Clinical Research Associate II Categories : Pharmaceuticals , Biotechnology , Science and Research
• Clinical Research Associate I Participates in the design, administration and monitoring of clinical trials. Analyzes and evaluates clinical data gathered during research. Ensures compliance with protocol and overall clinical objectives. Knowledge of FDA regulatory requirements is required. May require ACRP or SOCRA Clinical Research Professional exam completion. Requires a bachelor's degree in Science or its equivalent. Typically reports to a supervisor or manager. Work is closely managed. Works on projects/matters of limited complexity in a support role. Typically requires 0-2 years of related experience. View Clinical Research Associate I Salary Alternate Job Titles :Clinical Trails Research Associate I, Clinical Trials Data Analyst I, Clinical Research Associate I Categories : Pharmaceuticals , Biotechnology , Entry Level , Science and Research
• Clinical Research Manager Manages the clinical monitoring process and the administration of clinical trials. Supervises CRAs in in-house and on-site monitoring, filing, and clinical trial administration. Oversees adherence to SOPs, Good Clinical Practice and FDA regulations. Helps with the development and implementation of clinical processes, procedures, and programs. May require a master's degree in nursing. May require ACRP or SOCRA Clinical Research Professional exam completion. Typically reports to a director. Manages subordinate staff in the day-to-day performance of their jobs. True first level manager. Ensures that project/department milestones/goals are met and adhering to approved budgets. Has full authority for personnel actions. Typically requires 5 years experience in the related area as an individual contributor. 1-3 years supervisory experience may be required. Extensive knowledge of the function and department processes. View Clinical Research Manager Salary Alternate Job Titles :Clinical Research Programs Manager, Clinical Research Manager Categories : Pharmaceuticals , Biotechnology
• Research and Development Associate I Participates in research and development activities. Utilizes established mathematical and scientific techniques to compile and analyze data. Writes technical reports detailing procedures, outcomes, and observations. Requires a bachelor's degree. Typically reports to a supervisor or manager. Works on projects/matters of limited complexity in a support role. Work is closely managed. Typically requires 0-2 years of related experience. View Research and Development Associate I Salary Alternate Job Titles :R & D Support Associate I, Scientific Research Associate I, Research and Development Associate I Categories : Pharmaceuticals , Biotechnology , Energy and Utilities , Science and Research
• Research and Development Associate IV Participates in research and development activities. Utilizes established mathematical and scientific techniques to compile and analyze data. Writes technical reports detailing procedures, outcomes, and observations. May require a master's degree. Typically reports to a manager or head of a unit/department. Work is highly independent. May assume a team lead role for the work group. A specialist on complex technical and business matters. Typically requires 7+ years of related experience. View Research and Development Associate IV Salary Alternate Job Titles :R & D Support Associate IV, Scientific Research Associate IV, Research and Development Associate IV Categories : Pharmaceuticals , Biotechnology , Energy and Utilities , Science and Research
• Research and Development Associate V Participates in research and development activities. Utilizes established mathematical and scientific techniques to compile and analyze data. Writes technical reports detailing procedures, outcomes, and observations. May require a master's degree. Typically reports to a manager or head of a unit/department. Works autonomously. Goals are generally communicated in "solution" or project goal terms. May provide a leadership role for the work group through knowledge in the area of specialization. Works on advanced, complex technical projects or business issues requiring state of the art technical or industry knowledge. Typically requires 10+ years of related experience. View Research and Development Associate V Salary Alternate Job Titles :R & D Support Associate V, Scientific Research Associate V, Research and Development Associate V Categories : Pharmaceuticals , Biotechnology , Energy and Utilities , Science and Research
• Research and Development Associate II Participates in research and development activities. Utilizes established mathematical and scientific techniques to compile and analyze data. Writes technical reports detailing procedures, outcomes, and observations. Requires a bachelor's degree. Typically reports to a supervisor or manager. Gains exposure to some of the complex tasks within the job function. Occasionally directed in several aspects of the work. Typically requires 2 to 4 years of related experience. View Research and Development Associate II Salary Alternate Job Titles :R & D Support Associate II, Scientific Research Associate II, Research and Development Associate II Categories : Pharmaceuticals , Biotechnology , Energy and Utilities , Science and Research
• Research and Development Associate III Participates in research and development activities. Utilizes established mathematical and scientific techniques to compile and analyze data. Writes technical reports detailing procedures, outcomes, and observations. May require a master's degree. Typically reports to a supervisor or manager. Work is generally independent and collaborative in nature. Contributes to moderately complex aspects of a project. Typically requires 4-7 years of related experience. View Research and Development Associate III Salary Alternate Job Titles :R & D Support Associate III, Scientific Research Associate III, Research and Development Associate III Categories : Pharmaceuticals , Biotechnology , Energy and Utilities , Science and Research
• Scientist - Clinical Research Assumes lead role in various clinical research projects. Proposes, plans, organizes and executes experiments and research. Secures grants and funding for research and is responsible for controlling budgets. Summarizes findings in reports and communicates results. Interacts with other scientists within and outside of the organization. Provides recommendations that influence extensive clinical research activities. Requires an advanced degree. Typically reports to head of a unit/department. Work is generally independent and collaborative in nature. Contributes to moderately complex aspects of a project. Typically requires 4 -7 years of related experience. View Scientist - Clinical Research Salary Alternate Job Titles :Clinical Research Lead Scientist, Senior Clinical Researcher, Scientist - Clinical Research Categories : Science and Research , Biotechnology
• Clinical Research Director Directs and oversees the clinical research function for a healthcare organization. Develops research studies and creates standards and guidelines for clinical research services and programs. Ensures adherence to standard operating procedures, good clinical practice and FDA regulations. Requires an advanced degree. Typically reports to top management. Manages a departmental sub-function within a broader departmental function. Creates functional strategies and specific objectives for the sub-function and develops budgets/policies/procedures to support the functional infrastructure. Deep knowledge of the managed sub-function and solid knowledge of the overall departmental function. Typically requires 5+ years of managerial experience. View Clinical Research Director Salary Alternate Job Titles :Clinical Research Programs Director, Clinical Research Director Categories : Healthcare - Administrative , Science and Research

Clinical Research Associate Salary Estimate United States Nearby Locations...

Clinical research associate job title.

A Clinical Research Associate is responsible for running clinical trials, usually for an organization undertaking pharmacological drug testing. Will ensure that trials adhere to good clinical practice guidelines for monitoring clinical trials.

Salary Details

High demand job locations.

• Boston, MA - $69,183
• San Diego, CA - $97,846
• Philadelphia, PA - $58,054
• New York, NY - $90,654
• Los Angeles, CA - $94,281

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Clinical Research Associate Salary in the US

Clinical research associate - average salary, clinical research associate salary range, clinical research associate - salary differences, clinical research associate - pay by experience level in the united states, how work experience affects the salary of a clinical research associate, gender breakdown, clinical research associate - jobs by location, clinical research associate - related salaries.

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• United States

Clinical Research Associate

$86,960 (usd)/yr, $41.81 (usd) /hr, $1,939 (usd) /yr.

The average clinical research associate gross salary in United States is $86,960 or an equivalent hourly rate of $42. In addition, they earn an average bonus of $1,939. Salary estimates based on salary survey data collected directly from employers and anonymous employees in United States. An entry level clinical research associate (1-3 years of experience) earns an average salary of $62,280. On the other end, a senior level clinical research associate (8+ years of experience) earns an average salary of $107,310.

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$97,680 (USD)

Based on our compensation data, the estimated salary potential for Clinical Research Associate will increase 12 % over 5 years.

This chart displays the highest level of education for: Clinical Research Associate , the majority at 100% with bachelors.

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the United States

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Clinical Research Associate Salary - What's the pay for a clinic research associate?

Here's What You Need to Know to Get a Clinical Research Associate Job

What's the pay for a clinic research associate?: $61-$110K

A Clinical Research Associate (or Monitor) is hired either in-house (“the trial site”) or externally (by the sponsor or CRO) to do review clinical trial data and ensure that investigational therapies are tested ethically and scientifically through performing site visits that review files like patient medical notes in order to ensure quality of trial data. The catch 22 of clinical research associate jobs is that the ICH GCP guidelines require both education AND experience in order to work in this role, so you getting your foot in the door is tough. Once you get experience, your education (i.e. certifications or degrees showing understanding of additional responsibilities) can help promotes you quickly through the CRA career ladder.

How to become or get promoted as a clinical research associate?

Having a certification through CCRPS’s accredited Advanced Clinical Research Associate Certification course can help professionals 1) get promoted 2) get a raise 3) improve efficiency 4) get hired as a Clinical Research Associate.

How much does a Clinical Research Associate make in the United States?

The average Clinical Research Associate salary in the United States is $61-110K . Salary ranges can vary widely depending on many important factors, including education, certifications, additional skills, the number of years you have spent in your profession.

Clinical Research Associate (CRA) Salary

Per Payscale “An entry-level Clinical Research Associate (CRA) with less than 1 year experience can expect to earn an average total compensation (includes tips, bonus, and overtime pay) of $55,588 based on 203 salaries. An early career Clinical Research Associate (CRA) with 1-4 years of experience earns an average total compensation of $66,245 based on 1,118 salaries. A mid-career Clinical Research Associate (CRA) with 5-9 years of experience earns an average total compensation of $76,086 based on 294 salaries. An experienced Clinical Research Associate (CRA) with 10-19 years of experience earns an average total compensation of $81,540 based on 157 salaries. In their late career (20 years and higher), employees earn an average total compensation of $83,342.”

Determine CRA Salary by location using Payscale

CRA Career Progression - Indeed

Salary: Clinical Research Associate

Research Associate Salary resource: Click here to see the CRA Salary Range from 1,800+ employers

Clinical Research Associates Pay: Clinical Research Associate Salary in United States (by city)

Durham, NC - $97K

New York, NY, Irvine, CA, Houston, TX - $95K

Philadelphia, PA - $92K

Atlanta, GA - $84K

Raleigh, NC - $82K

Chicago, IL - $79K

Payscale: CRA Career Pathway

Senior Clinical Research Associate Salary

The average salary of a Senior Senior Clinical Research Associate is ~105K per year ($54/hour, $2k/week, $9k/month). This can range from $81k to $139k.

Glassdoor Salary range for Senior CRAs

Starting Salary of a Clinical Research Associate Position is between $60,000 and $65,000

Some employers may prefer hiring entry-level clinical research associates with less experience in clinical research so they can learn their job functions by training under Senior CRAs or CRA IIs.

Clinical Research Associate II Salary is $86,677 / yr

CRA II @ PPD: $84,733 /yr

CRA II @ PRA Health Sciences: $96,017 /yr

CRA II @ IQVIA: $79,412 /yr

CRA II @ ICON: $100,000 /yr

Comment below how much you get paid and what helped you get promoted!

Clinical Research Associate vs Coordinator (CRA vs CRC)

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Clinical Research Associate - Home-Based (Southeast)

• Location: United States
• Categories Clinical Monitoring
• __vacancyopjusttionswidget.opt-Business Area__ ICON Strategic Solutions
• __vacancyopjusttionswidget.opt-Remote Working __ Remote

About the role

ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.

The Clinical Research Associate (CRA) monitors the progress of clinical studies at investigative sites or remotely, ensuring clinical trials are conducted, recorded, and reported in accordance with the protocol, standard operating procedures (SOPs), International Conference on Harmonization Good Clinical Practices (ICH-GCP) and all applicable regulatory requirements.

• Completes onsite and remote monitoring activities in accordance with all ICH-GCP guidelines, applicable regulations, SOPs, and study processes. Activities include qualifying potential investigative sites, initiating clinical trials, maintaining study files, and providing instructions to site personnel and study close out.
• Verifies the protection of study participants by confirming informed consent procedures and protocol have been performed in accordance to applicable regulations.
• Ensures the integrity of clinical data and that the study is conducted in compliance with the approved protocol, GCP, applicable regulations, and SOPs.
• Manages the investigative site staff to facilitate trial deliverables, e.g., subject enrollment, data deliverables.
• Verifies proper management and accountability of Investigational Product (IP).
• Writes and submits reports of investigational site findings and updates applicable tracking systems. Escalates observed deficiencies, issues, and corrective and preventative action plans as appropriate.
• Manages essential documents as required by local regulations and ICH-GCP guidelines before, during, and after a clinical study; assists with resolution of investigational site/data queries.
• Performs key risk assessment and management responsibilities throughout the project, including key risk indicator and site health analysis, site process evaluation, and project escalation.
• Participates in audit preparation and follow-up activities as needed.
• Independently performs a variety of onsite and offsite monitoring visit types.
• Gathers and reviews information for assigned sites and identifies inconsistencies. With limited guidance from project and functional management, assesses risk and escalates as appropriate.
• Assists with non-complex ad hoc, short-term assignments in support of additional studies or departmental initiatives.
• May serve as preceptor, providing training to less experienced clinical team members
• 2 years of experience supporting clinical trials including 1 year of on-site monitoring experience
• In-depth knowledge of the drug development process
• In-depth knowledge and practical utilization of ICH- GCP and applicable regulatory requirements
• Sound knowledge of applicable policies and procedures, SOPs, work instructions and other guidance documents
• Good spoken and written communication skills; good presentation skills
• Strong interpersonal, collaboration and time management skills
• High proficiency with Microsoft Office and company collaboration applications
• Excellent skill in the utilization of applicable clinical systems
• Excellent critical thinking skills
• Excellent organizational skills
• Ability to focus on detail for extended periods of time; high attention to accuracy
• Ability to travel extensively
• Ability to establish and maintain effective working relationships with investigative site staff
• Equivalent combination of education, training and relevant experience may be considered in place of the education and experience stated above. All employees must read, write and speak fluent English and host country language.

What ICON can offer you: Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family. Our benefits examples include:

• Various annual leave entitlements
• A range of health insurance offerings to suit you and your family’s needs
• Competitive retirement planning offerings to maximise savings and plan with confidence for the years ahead
• Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family’s well-being
• Life assurance
• Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others

Visit our careers website to read more about the benefits of working at ICON: https://careers.iconplc.com/benefits At ICON, diversity, inclusion & belonging are fundamental to our culture and values. Our rich diversity makes us more innovative which helps us better serve our people, patients, customers, and our communities. We're proud of our diverse workforce and the work we’ve done to become a more inclusive organisation. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know through the form below. https://careers.iconplc.com/reasonable-accommodations Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.

**Actual compensation will be determined based on factors such as geographic location, work experience, education/training, and skill level.**

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To excel as a Clinical Research Associate (CRA) in a Clinical Research Organization (CRO), you need a combination of education, skills, and the right mindset. Brazil-based CRA II Debora shares her

Brazil-based CRA II Debora Oh shares her tips on how to become a great CRA and provides insight into life at ICON.

Unlocking your Potential: The Benefits of ICON’s EPIC Internship Program  Internship programs have become a vital stepping stone for students and young professionals seeking to gain practic

Read more about ICON plc's EPIC (Entry-level Professionals in CRO (Contract Research Organization)) internship program.

How to progress as a Clinical Research AssociateTo thrive as a Clinical Research Associate (CRA), it is imperative to cultivate a multifaceted skill set and demonstrate unwavering commitment to exce

 Senior CRA Yemi Moses recounts her development and shares her career ambitions with ICON plc.

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Senior Clinical Research Associate Salary in the United States

Senior clinical research associate salary.

How much does a Senior Clinical Research Associate make in the United States? The average Senior Clinical Research Associate salary in the United States is $87,700 as of March 26, 2024, but the salary range typically falls between $76,357 and $100,456 . Salary ranges can vary widely depending on many important factors, including education , certifications, additional skills, the number of years you have spent in your profession. With more online, real-time compensation data than any other website, Salary.com helps you determine your exact pay target.

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Clinical Data Associate- Research

• Jacksonville, FL

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This Hybrid/Remote position supports the Mayo Clinic Research's clinical trials and research studies. You will be part of a larger team that brings innovation and advances to healthcare.

Under the direct supervision of the study team and research leadership, assists in coordinating the details of the study and documentation concerning study protocols, patient scheduling, retrospective & prospective chart work, data collection, data entry, data management, follow-up information, and compliance with federal, state, sponsor, and institutional guidelines. 

Overview for the Clinical Data Associate I (CDA I): 

• The CDA I provides data management support for clinical trials. 
• The CDA I is responsible for data collection in a timely manner by performing data abstraction of clinical and demographic information from the electronic medical record and case report forms into the study specific electronic data capture system, as well as leading and assisting the data team in their roles. 
• The CDA I manages the study database as directed. 
• The CDA I performs other administrative duties related to the study as assigned including creation of source documents, redaction of protected patient information under HIPAA privacy laws, and sending/faxing query resolutions to industry sponsors or CRO personnel. 
• The CDA I is responsible for scheduling clinical research monitor visits, maintaining the monitor visit calendar, and serving as the campus visitor escort to pharmacy, radiology, BAP Lab, and other locations on campus, as needed. 
• The CDA I independently prioritizes assignments and completes ongoing tasks following established research regulatory guidelines and best practices, and may assist with general office responsibilities or research related projects. 
• CDA I’s perform administrative functions to support work unit and maintain continuing education requirements as required for the position by the completion of Human Subject Protection and Good Clinical Practice (GCP) trainings at initial employment and every 3 years thereafter

During the selection process you may participate in an OnDemand (pre-recorded) interview that you can complete at your convenience. During the OnDemand interview, a question will appear on your screen, and you will have time to consider each question before responding. You will have the opportunity to re-record your answer to each question — Mayo Clinic will only see the final recording. The complete interview will be reviewed by a Mayo Clinic staff member and you will be notified of next steps .

High School Diploma with medical terminology or clinical experience preferred. 

Prior data entry, Excel, Outlook mail/calendar and Adobe Acrobat pro experience preferred. Excellent written, oral, and interpersonal communication skills are a must. 

A candidate must possess high attention to detail and have demonstrated critical thinking skills.

This position is not eligible for visa sponsorship.  Mayo does not participate in OPT Stem. 

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Baxter looking for Research Associate, M.Pharm, MSc Apply

Baxter provides a broad portfolio of essential renal and hospital products, including home, acute and in-centre dialysis; sterile IV solutions; infusion systems and devices; parenteral nutrition; surgery products and anesthetics; and pharmacy automation, software and services. The company’s global footprint and the critical nature of its products and services play a key role in expanding access to healthcare in emerging and developed countries.

Post : Research Associate III (Hybrid)

Job Responsibilities • Act as Product Risk Management Owner (PRMO) for Kidney care products • Understand the PRMO risk management process and drive periodic risk reviews in a timely manner to avoid any non compliance • Support the Product Design Owners, Technical leaders, Change Control owners for any updates to the risk files (Design failure mode effect analysis (DFMEA), Process failure mode effect analysis (PFMEA) and other required documents • Support the event based risk review products for the products of interest • Collaborate with the product design owners, technical experts and all the key stakeholders at a global front for implementing the risk management plan for both the Sustaining Organization and New Product Development projects • Organize, plan and execute activities in compliance with current QA/ environmental/ regulations and standards

• Co-ordinate with all the global plants and actively participate in quality reviews to monitor the complaints, process or design related changes and associated failure modes • Organize, plan and follow the execution of product changes, supplier changes and labelling tasks related to life cycle management projects • Ensure good internal and cross-functional communication at a global front and regular status update of projects.

Candidate Profile • Master’s in chemistry or M. Pharm. with at 9+ years of relevant experience • Excellent English verbal and written communication skills • Exposure to medical devices and drug products • Good knowledge of product development stages and life cycle management: development, stability, clinical, registration, process transfer, production, suppliers, customer service • Good knowledge of Design Control documentation and process • Good knowledge of risk management process of drug products and medical devices

• Demonstrated project/program leadership in drug/pharmaceutical products • Working knowledge of international/regional/national regulations and standards • Experience in project management and stakeholder management at a global front • Must be able to able to carry out strategy and vision set by upper management and be able to communicate the vision to more junior associates. • Ability to work independently. Equal Employment Opportunity Baxter is an equal opportunity employer. Baxter evaluates qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, disability/handicap status or any other legally protected characteristic.

Additional Information   Experience : 9+ years Qualification : MSc, M.Pharm Location : Bengaluru, Karnataka, India Industry Type : Pharma/ Healthcare/ Clinical research Job Category : Regulatory Affairs  End Date : 30th April 2024

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