Clinical Trial Project Manager Job at Medasource, Sacramento, CA

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  • Medasource
  • Sacramento, CA

Job Description

Position: Clinical Trial Project Manager

Start Date: ASAP

Location: North Valley, CA (80% at Sacramento Morse St. site, 20% at South Sacramento site, a 20–30-minute drive)

Contract: 6 months-1 year, M-F (40 hours/week)

Responsibilities:

  • Oversee the execution of 5-6 clinical studies in their final or follow-up phases, while providing support for newer studies.
  • Manage trial preparation, including organizing supplies, equipment, and investigator training.
  • Lead and mentor staff to address challenges, ensuring minimal oversight is required.
  • Operate effectively in limited space while managing high supply volumes.
  • Ensure strict compliance with HIPAA , FDA regulations , GCP , and other regulatory requirements.
  • Monitor and support studies in the dermatology , stroke , and cardiology therapeutic areas.
  • Coordinate site visits, spending 80% of time at the Sacramento Morse St. location and 20% at the South Sacramento site.

Requirements:

  • Bachelor’s degree in a related field.
  • Proven clinical trial experience, particularly in operational roles.
  • Strong knowledge of GCP , HIPAA , compliance requirements, and regulatory audits.
  • Familiarity with EDC systems like Epic or RedCap.
  • Experience managing high-intensity teams and complex projects.
  • Ideal candidates have backgrounds from Stanford , UCSF , or UC Davis , with a proven understanding of clinical trial processes.

Preferred Skills and Experience:

  • Demonstrated experience in risk-based monitoring and implementing CAPAs .
  • Knowledge of regulatory audits, IRB, and SOPs.
  • Strong conflict resolution and task prioritization skills.

Job Tags

Contract work, Immediate start,

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