Clinical Trial Manager - Remote

Job type:
Real Staffing
San Francisco
flag_no USA
project ID:

This project is archived and not active any more.
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Primary Responsibilities and Duties:
  • Conducts and/or oversees all aspects required for selecting, initiating, monitoring and closing investigational sites in accordance with all applicable SOPs and GCP/ICH requirements.
  • Serves as a primary contact for internal study team members and external vendors and clinical sites.
  • Provides oversight of Clinical Research Organization (CRO) interactions in the areas of study/project management, monitoring, site management, trial master files, and data management.
  • Assists in the preparation of clinical trial documents, including study protocols, amendments, model ICFs, laboratory manuals, CRF completion guidelines, study specific instructions, etc.
  • Provides timely and accurate information to Project Management for program level tracking.
  • Participates in evaluating study drug supply requirements and manages the logistical aspects of distributing supplies to the investigational sites.
  • Coordinates investigator meetings and develops presentation materials.
  • Routinely reviews study data and progress of EDC entry; works with data management and clinical sites to resolve data discrepancies.
  • Identifies program/clinical trial risks; proactively suggests and implements mitigation strategies.
  • Participates in the evaluation, selection and eventual management of vendors.
  • Participates in the preparation and finalization of Galena Biopharma SOPs.
  • Performs job duties with minimal supervision and has a sound critical thinking and problem solving skills.
  • Ability to travel up to 30%.


Qualifications include a BA or BS within a scientific discipline, or an equivalent combination of education and work experience. Minimum of five years related experience and/or training, four of which include Clinical Research Associate with lead CRA or Team Leader experience. A strong medical/science background with oncology experience. Prior global trial experience required. Knowledge of GCP/FDA/ICH regulations required.

The eligible candidate needs to reside in SFO bay area.