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 oversee all regulatory tasks for assigned studies
• Involved in studies from start-up through maintenance and closeout

Required Qualifications

• 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 in Informed Consent and Regulatory document review required