Senior Clinical Research Associate - West Coast - FSP
Employment type
Full-time
Work setting
On-site
Location
Providence, RI
Schedule
Day shift
Posted
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Job overview
The Senior Clinical Research Associate is an onsite role based in Providence, RI. Compensation is not specified in the posting, and this position supports Parexel's clinical trial operations. This role exists to manage investigator sites, monitor clinical trials, and ensure patient safety and data quality in accordance with Good Clinical Practices (GCP) and sponsor standards. The associate acts as the primary point of contact for sites and facilitates study execution from activation to close-out.
What you'll do
- Manage site monitoring and close-out activities.
- Ensure compliance with study protocols and GCP.
- Resolve protocol-related issues.
- Monitor adverse events and collaborate with the Drug Safety Unit.
- Submit required documentation and metrics.
What we're looking for
- Skills & competencies
- full-timeday shiftprovidence riparexelclinical researchgcpsite monitoringonsitebachelor's degree requiredtravel required
- Work arrangement
- Weekend coverage required
Why this role
Requires 3+ years of monitoring experience, preferably in Oncology.
About the employer
Parexel is hiring for this role. Industry: Research and Development in the Physical, Engineering, and Life Sciences (except Nanotechnology and Biotechnology). Sector: 54.
Additional details
- Industry sector
- 54
- Industry
- Research and Development in the Physical, Engineering, and Life Sciences (except Nanotechnology and Biotechnology)
- Occupation code
- 15-2051.02
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Listing ID: 8a7a1943-cb33-478f-8f34-ca9586bee584