Study Start-Up Associate
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 and Education 1-4 years of prior work experience in oncology clinical trials Experience with randomized (larger) trials is required Prior experience in a CRO/pharmaceutical environment is preferred Experience with Informed Consent and Regulatory document review is required Proficient knowledge of Word and Excel
