Clinical Research Associate II
Parexel(2 months ago)
About this role
This role at Parexel serves as the primary point of contact for assigned clinical trial sites across the full site lifecycle, from feasibility and start-up through maintenance and close-out. The position focuses on ensuring effective site engagement and smooth study implementation while supporting timely progression of clinical trials that improve patient health.
Required Skills
- Site Start-Up
- Site Management
- Feasibility Assessment
- Regulatory Submissions
- IRB/IEC Coordination
- Informed Consent
- Contract Negotiation
- CTMS
- TMF Management
- EDC
+14 more
Qualifications
- Bachelor's Degree
- Nursing Qualification
- Driver's License
About Parexel
parexel.comFor over 35 years Parexel has been a trusted global CRO and biopharmaceutical services company. Learn more about how we can help.
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