Senior Clinical Research Associate
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About the role
ProTrials seeks a Senior Clinical Research Associate to monitor and manage clinical trials, including site visits, source-data review, investigational product oversight, regulatory documentation, and data issue resolution. The role is remote, may require travel up to 65%, and supports CRA I and CRA II staff. Qualifications include RN or a bachelor’s/advanced degree in biological sciences or a related field, or an equivalent combination of experience, education, or training with previous CRA experience.
Key requirements
- • RN or Bachelor and/or advanced degree in biological sciences or related field, or equivalent combination of relevant experience, education or training, and previous CRA experience demonstrating career growth in the CRA position
- • Required skills: Clinical trial monitoring, Clinical trial site qualification, initiation, interim, and close-out visits, Site personnel training, Investigational product and supply management, Laboratory sample management, Source data and case report form review, Data query and discrepancy resolution, Regulatory document review, Study file management, Knowledge of FDA regulations and practical implementation, Familiarity with medical and pharmaceutical industries, Microsoft Word, Excel, and PowerPoint, Ability to travel, including by air or car on short notice
Opportunity details
- • Workplace: Remote
- • Posted: Oct 1, 2026
- • Original advert language: English
Full vacancy
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See original vacancy ↗Employer’s role description
Job title: Senior Clinical Research Associate
Team: Clinical Operations
Location: Regional
All locations: Regional
Work type: Full Time
Workplace type: remote
Salary range: USD 130000 – 155000; per year
ProTrials is a women-owned, WBENC-certified Contract Research Organization (CRO) that has been a trusted partner in clinical research since 1996. Founded with a clear mission to deliver high-quality, experienced, and ethical services, we’ve supported research behind innovative treatments in the pharmaceutical, biotech, and medical device industries.
Our people are the heart of everything we do. We believe great work happens when team members feel valued, supported, and empowered. At ProTrials, you’ll join a collaborative community committed to making a meaningful impact on global health.
We are excited to connect with skilled individuals who share our passion for advancing clinical research with care, integrity, and excellence.
ABOUT THE JOB
The Senior Clinical Research Associate (Sr. CRA) plays an integral part in the successful monitoring and management of clinical trials. Responsibilities of a Sr. CRA include ensuring clinical trials are conducted, recorded, and reported in accordance with the protocol, standard operating procedures (SOPs), ICH GCP, and all applicable regulatory requirements. Sr. CRAs may be required to travel up to 65%.
HERE IS WHAT YOU WILL DO:
- Monitor clinical studies of investigational and approved products that have been determined to satisfy a medical need and/or offer a commercial benefit, including qualification, initiation, interim, and close-out site visits
- Manage and train site personnel on therapeutic area, protocol requirements, proper source documentation, and case report form completion
- Manage and track the preparation and return of investigational supplies at individual sites
- Monitor and document investigational product dispensing, inventory, and reconciliation
- Monitor and document laboratory sample storage and shipment
- Monitor trial by reviewing and reporting on the following: site enrollment and termination updates, monitoring visits, protocol deviations/exceptions, serious adverse events, and laboratory abnormalities
- Review source data and case report forms for accuracy, completeness, and integrity of the data, and identify and resolve ongoing data issues
- Review data queries and listings, and work with study centers to resolve data discrepancies
- Review regulatory documentation for accuracy and completeness, and support study centers with regulatory issues
- Maintain complete and accurate study files and review files to ensure all appropriate documentation is present
Verification
- ✓ Employer verification
- ✓ Original posting located
- Last verified: Oct 4, 2026