Senior Clinical Research Associate - Contract Position
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About the role
ProTrials seeks a contract Senior Clinical Research Associate to monitor and manage clinical trials, conduct site visits, support site personnel, review trial data and regulatory documentation, and maintain study files. The role is remote, may require up to 65% travel, and requires an RN or relevant biological sciences degree or an equivalent combination of experience, education or training and previous CRA career growth.
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 management, Site qualification, initiation, interim and close-out visits, Site personnel training, Investigational product accountability, Laboratory sample monitoring, Source data and case report form review, Data query and discrepancy resolution, Regulatory document review, Study file management, Knowledge of FDA regulations, Ability to travel on short notice, Microsoft Word, Excel and PowerPoint
Opportunity details
- • Workplace: Remote
- • Employment: Contract
- • 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 - Contract Position
Team: Clinical Operations
Location: Regional
All locations: Regional
Work type: Contract
Workplace type: remote
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
ProTrials is seeking a Contract Senior Clinical Research Associate to join our team.
The Contract Senior Clinical Research Associate (Sr. CRA) plays an integral part in the successful monitoring and management of clinical trials. Responsibilities of a Contract 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. Contract 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
Verification
- ✓ Employer verification
- ✓ Original posting located
- Last verified: Oct 4, 2026