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Clinical Research Associate (CRA) careers in the USA with the FSP team at ICON
Apply for Clinical Research Associate (CRA) jobs with ICON, the world's largest provider of Functional Service Provision (FSP). We provide global strategic resourcing and FSP services to the biopharmaceutical and medical device industries. With more than 60 FSP solutions across all major functions from clinical monitoring and project management through data management, statistical programming now is a perfect time to join our team.
Why join the FSP team at ICON?
Working at ICON is more than a job, it’s a calling for people who care and are passionate about improving patients’ lives. At ICON, we care about our people and your passion, you are key to our success. We aim to provide an open and friendly work environment where we empower our people and provide them with opportunities to develop their long-term career.
It takes courage to move from one job to another, the process involves careful consideration. Reach out having the conversation that would change your life and the lives of our patients. Our team of recruitment experts will provide the information you need in making the right decision.
At ICON you will have the opportunity to work with one of the global top 20 pharmaceutical companies, working on novel therapies that deliver real impact. If you want a career with a difference, ICON is the place for you.
We have a range of job vacancies across the USA as well contract and homebased roles for experienced CRAs, CRA IIs and Senior CRAs.
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Clinical Research Associate
- Location: Italy
- Categories Clinical Monitoring
- __vacancyopjusttionswidget.opt-Business Area__ ICON Strategic Solutions
- __vacancyopjusttionswidget.opt-Remote Working __ Remote
TA Business Partner
- Icon Strategic Solutions
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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 Field CRA is responsible for monitoring and management of clinical sites. This position focuses on all activities required to evaluate, initiate, monitor and close clinical sites in compliance with the Code of Federal Regulations and ICH/GCP Guidelines.
We are currently looking for a Clinical Research Associate to join one of our Sponsor-dedicated teams.
Principal Responsibilities:
- Act as liaison between the in-house team, vendors, and multiple clinical sites.
- Develop strong site relationships, maintaining close contact with sites by telephone, correspondence, and remote and on-site visits.
- Apply SOPs, Clinical Monitoring Plan (CMP), protocols, study manuals, other study materials as applicable.
- Help identify and qualify potential investigators. Perform Pre-Study Site Visits.
- Assist with start-up activities, including essential document review and collection as requested.
- Perform Site Initiation Visits, Interim Monitoring Visits,Close Out visits as assigned.
- Provide initial and ongoing training to clinical investigators and other site staff regarding the study protocol, procedures, documentation, as well as regulatory requirements.
- Monitor site compliance with study protocol and GCP.
- Perform source data review and verify adequacy of clinical data through comparison of case report forms to source documents per CMP.
- Ensure the site is entering data according to the CRF Completion Guidelines and meeting data entry and query resolution deadlines.
- Perform drug accountability and ensure adequate drug supply.
- Review research specimen sample documentation, storage and processing, and ensure shipments are sent to central lab as required.
- Assist study team as necessary in resolving lab queries and other issues.
- Collaborate with the drug safety group to ensure site compliance with serious adverse event reporting requirements.
- Ensure adequacy of clinical supplies to the site.
- Collect and review site essential documents and ensure site regulatory files are complete and accurate.
- Monitor site compliance with IRB policies/processes and ensure timely reporting, submissions, and approvals.
- Track and report progress of study, data monitoring, protocol variations, issue resolution, and follow up compliance.
- Prepare and complete visit trip reports, confirmation and follow up letters within timelines outlined in the CMP.
- Track, report, and follow all action items to resolution.
- Maintain CTMS in a timely fashion, utilizing available reports and study tools.
- Work proactively with sites to address site issues and action items to obtain swift resolution and escalate to PL/PI per CMP.
- Assist data management as required.
- Provide co-monitoring support as requested or as necessary to develop additional skills
Dedicated, collaborative and inspire others.
Here at ICON we want our employees to succeed and ensure that they are set up for this success through constant training, development and support. To enable success in this position you will have:
- BA/BS, or equivalent, or a minimum 2 years of other relevant experience and training. Prior monitoring experience is mandatory.
- Knowledge of and ability to apply CFR and GCP/ICH is required. Experience on global clinical trials is preferred.
- Proficiency with Microsoft Office Products: Word, Excel, PowerPoint, SharePoint (preferred). Previous experience with EDC and CTMS systems.
- Requires effective organizational and time management skills.
- Able to manage multiple and varied tasks with enthusiasm under limited direction and on own initiative. Ability to prioritize workload with attention to detail.
- Strong communication and interpersonal skills.
- Ability to discuss scientific, medical and therapeutic area information within small and large groups of medical professionals.
- Flexibility towards work assignments, learning, and travel.
- . Travel requirements will vary depending on study requirements, site assignments, site remote monitoring capabilities, and geographical location.
- Responsive and proactive, a team player.
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 ICON, including subsidiaries, is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, colour, 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 or submit a request here . 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.
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The estimated total pay range for a Clinical Research Associate at ICON is $82K-$115K per year, which includes base salary and additional pay. The average Clinical Research Associate base salary at ICON is $97K per year. The average additional pay is $0 per year, which could include cash bonus, stock, commission, profit sharing or tips.
Our Clinical Research Associates (CRAs) are at the heart of our success. CRA's work closely with pharmaceutical companies, clinical contractors and hospitals, ensuring adherence to regulations and principles from phases II-IV of a clinical trial. Our CRAs are at the core of everything we do at ICON.
Average ICON plc Clinical Research Associate yearly pay in the United States is approximately $102,141, which is 12% above the national average. Salary information comes from 471 data points collected directly from employees, users, and past and present job advertisements on Indeed in the past 36 months. Please note that all salary figures are ...
Apply for Clinical Research Associate (CRA) jobs with ICON, the world's largest provider of Functional Service Provision (FSP). We provide global strategic resourcing and FSP services to the biopharmaceutical and medical device industries. With more than 60 FSP solutions across all major functions from clinical monitoring and project management ...
Clinical Research Associate- CA/AZ. ICON. Remote. $89,372 - $111,720 a year. ICON plc is a world-leading healthcare intelligence and clinical research organization. Excellent skill in the utilization of applicable clinical systems. Posted 10 days ago ·. More...
The average ICON plc salary ranges from approximately $42,634 per year for Documentation Manager to $190,309 per year for Senior Account Director. Average ICON plc hourly pay ranges from approximately $15.00 per hour for Management Assistant to $72.32 per hour for Director of Regulatory Affairs. ... Clinical Research Associate. $102,141 per ...
Salaries at Icon Clinical Research Inc range from an average of $63,135 to $158,284 a year. Icon Clinical Research Inc employees with the job title Clinical Trial Manager make the most with an ...
Avg. Base Salary ( USD) 25%. $104k. MEDIAN. $110k. 75%. $121k. The average salary for a Senior Clinical Research Associate (CRA) is $110,498 in 2024. Base Salary.
The average salary for Clinical Research Associate is $73,209 per year in the Canada. The average additional cash compensation for a Clinical Research Associate in the Canada is $4,000, with a range from $1,734 - $9,230. Salaries estimates are based on 182 salaries submitted anonymously to Glassdoor by Clinical Research Associate employees in ...
Average ICON plc Research Associate hourly pay in the United States is approximately $19.12, which is 28% below the national average. Salary information comes from 62 data points collected directly from employees, users, and past and present job advertisements on Indeed in the past 36 months. Please note that all salary figures are ...
Average ICON plc Clinical Research Associate yearly pay in the United Kingdom is approximately £42,934, which is 30% above the national average. Salary information comes from 57 data points collected directly from employees, users, and past and present job advertisements on Indeed in the past 36 months.
The estimated total pay range for a Clinical Research Associate at ICON is $84K-$103K per year, which includes base salary and additional pay. The average Clinical Research Associate base salary at ICON is $89K per year. The average additional pay is $18K per year, which could include cash bonus, stock, commission, profit sharing or tips.
Average ICON plc Clinical Research Coordinator yearly pay in the United States is approximately $55,961, which meets the national average. Salary information comes from 54 data points collected directly from employees, users, and past and present job advertisements on Indeed in the past 36 months. Please note that all salary figures are ...
Clinical Research Associate - 12 month FTC. UK. ICON Strategic Solutions. Clinical Monitoring. Read more. Clinical Data Science Associate. Swansea. ICON Full Service & Corporate Support. Clinical Data Management.
As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas.
The estimated total pay range for a Clinical Research Associate at ICON is $79K-$122K per year, which includes base salary and additional pay. The average Clinical Research Associate base salary at ICON is $88K per year. The average additional pay is $0 per year, which could include cash bonus, stock, commission, profit sharing or tips.
About the role ICON and you Application Process Day in the life Who we are. Clinical Research Associate. Location: France. Reference:2024-108887. Categories Clinical Monitoring. __vacancyopjusttionswidget.opt-Business Area__ ICON Strategic Solutions. Hi, I am Theo and I manage this role.
The estimated total pay range for a Clinical Research Associate at ICON is £35K-£42K per year, which includes base salary and additional pay. The average Clinical Research Associate base salary at ICON is £37K per year. The average additional pay is £0 per year, which could include cash bonus, stock, commission, profit sharing or tips.
The estimated total pay range for a Clinical Research Associate at ICON is ₹2L-₹9L per year, which includes base salary and additional pay. The average Clinical Research Associate base salary at ICON is ₹4L per year. The average additional pay is ₹0 per year, which could include cash bonus, stock, commission, profit sharing or tips.
We are currently looking for a Clinical Research Associate to join one of our Sponsor-dedicated teams. Principal Responsibilities: Act as liaison between the in-house team, vendors, and multiple clinical sites. Develop strong site relationships, maintaining close contact with sites by telephone, correspondence, and remote and on-site visits.