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Clinical Trial Operations Consultant

Medasource
Pleasanton, CA Full Time
POSTED ON 4/26/2025
AVAILABLE BEFORE 5/25/2025

Title : Clinical Trial Feasibility / Operations Consultant

Start Date : ASAP

Location : Pleasanton, CA

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

The Clinical Trial Feasibility / Operations Consultant will work with a team under direct supervision of the Clinical Trials Operations Manager.

Responsibilities :

  • Determine study activities related to clinical trial protocols.
  • Work with principal investigators and study teams in clinical trial start up activities.
  • Address logistical issues in order to launch clinical trials in medical facilities
  • Must demonstrate excellent organizational, interpersonal, and communication skills
  • Other duties as required to assist launching clinical trials.

Requirements :

  • Bachelor's Degree in related field
  • Must demonstrate excellent organizational, interpersonal, and communication skills.
  • Experience with implementing / coordinating clinical trials
  • Familiarity with medical terminology
  • Must be able to work in a Labor / Management Partnership environment.
  • Experience with word-processing and spreadsheet software programs

    • Soft Skills :

  • Must be dependable, punctual, detail-oriented, and able to follow detailed protocols precisely.
  • Experience with research administration.
  • Must be able to work successfully with a wide variety of internal and external project staff and research participants
  • Must exhibit a professional manner with a high degree of courtesy, tact, and sensitivity.
  • Must be able to work well independently as well as part of a larger multi-disciplinary research team.

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