Clinical Trial Associate II
Posted on :
30-12-2023
Employer Active
1 Vacancy
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Job Description
Req ID : 2205966
- Ensure study documentation, communication, training and data collection is aligned with study protocol adherence, and all applicable SOPs, regulations and guidelines
- Lead the development of assigned study-related documents (e.g., informed consent, source documents, study logs, etc.).
- Participate in all phases of clinical trial site management from study start-up, through study conduct and completing closeout activities.
- Collect and review site regulatory documents for accuracy and completion (1572, Financial Disclosure documents, CLIA waivers, etc.)
- Prepare essential documents package to support investigational product release for study and site approval as well as applicable study and site continuity report submissions and close-out submissions.
Employment Type
Remote
Company Industry
Department / Functional Area
Key Skills
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