Clinical Trials Activator

Job Summary

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 conduct

Required qualifications

• Bachelor'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