About The Position

Do you enjoy working in a fast-paced environment where you are empowered to make strategic decisions and contribute to a growing and profitable company? Join us at Medpace! Our clinical operations activities are growing rapidly, and we are currently seeking a full-time, Global Study Start-Up Project Manager to join our Clinical Operations team. This position plays a key role in the clinical trial management process at Medpace. Incentives can include: Competitive bonus program, sign-on bonus, and equity awards.

Requirements

  • Bachelor's degree required, advanced degree in Life Sciences preferred
  • 5+ years of experience in clinical research, preferably in a Senior/Lead role at a CRO in Study Start-Up
  • Project management experience and demonstrated role in developing others
  • Strong oral and written communication skills required

Responsibilities

  • Efficiently manage successful execution of global start-up, maintenance, and close-out studies;
  • Effectively lead others in a matrix environment;
  • Perform quality checks on submission documents and site essential documents;
  • Prepare and approve informed consent forms;
  • Serve as a Sponsor point of contact for start-up and regulatory submissions items;
  • Review pertinent regulations to develop proactive solutions to start-up challenges;
  • Prepare new business proposals and present during bid defenses, general capabilities meetings, and audits;
  • Contribute to the growth and development of departmental staff, processes and systems.

Benefits

  • Flexible work environment
  • Competitive PTO packages – starting at 20+ days
  • Company-sponsored employee appreciation events
  • Employee health and wellness initiatives
  • Competitive compensation and benefits package
  • Structured career paths with opportunities for professional growth
  • Discounts for local businesses
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