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Study Start-Up Associate

virtual vocationsNew York, NYSenior L5
Working remotely in a full-time capacity, the Study Start-Up Associate will manage the end-to-end coordination of study start-up activities, including site identification, regulatory submissions, and stakeholder engagement while ensuring timely and high-quality project delivery.
Key responsibilities: Participates in the start-up process through site activation, providing customer service to internal and external parties Collaborates on trial feasibility processes and maintains SSU trackers and documentation Supports the preparation and execution of regulatory and IRB/IEC submissions and approvalsRequired qualificationsBachelor's Degree with at least 1 year of experience in a clinical research setting, preferably within a CRO Good knowledge of clinical research processes and medical terminology Basic understanding of regulatory and IRB/IEC submission processes Working knowledge of current ICH GCP guidelines and applicable regulations Ability to manage multiple competing priorities within various clinical trials
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Level

Senior L5

Location

New York, NY

Occupation

Clinical Research Coordinators

Industry

Research and Development in Biotechnology

Posted

2 days ago

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