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Study Start-Up Associate
Job Summary
A company is looking for a Study Start-Up Associate I or II, level dependent upon experience.
Key Responsibilities
- Serve as the primary point of contact to study sites during start-up
- Manage multiple clinical study protocols and regulatory tasks for assigned studies
- Participate in studies from start-up through maintenance and closeout
Required Qualifications, Training, and Education
- 1-4 years of prior work experience required
- Oncology clinical trials experience required
- Experience with randomized (larger) trials required
- Prior experience in a CRO/pharmaceutical environment preferred
- Experience with Informed Consent and Regulatory document review required
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COMPLETE JOB DESCRIPTION
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Company Overview
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