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About the role

Managing the startup of new clinical trials, the full-time Clinical Trials Activator will ensure adherence to institutional policies and activation timelines while collaborating with key stakeholders in a remote work environment.
Key responsibilities: Lead the study activation process, tracking and reporting progress on activation tasks and milestones Drive collaboration and accountability among investigators, research teams, and external sponsors to optimize the study startup process Prepare essential research materials and documentation, ensuring compliance and readiness for study conductRequired qualificationsBachelor's degree with three years of experience in clinical trials, or an associate's degree with five years, or a high school diploma with seven years of relevant experience Clinical Research Certification (CCRP or CCRC) or Certified Associate in Project Management (CAPM), with the ability to obtain certification within one year of starting the position Experience in patient-facing coordination, data management, or regulatory aspects of clinical research

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JOB OVERVIEW

Experience level

Mid

Location

New York, NY

Occupation

Clinical Research Coordinators

Industry

Research and Development in the Physical, Engineering, and Life Sciences

Posted

yesterday

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