Location: Redwood City, California, USA
Salary: US$40 - US$47 per hour + competitive
Job Type: Contract
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  • BS/BA in a relevant scientific discipline is preferred
  • Minimum 0-2 years related experience, preferably in the pharmaceutical industry or equivalent
  • Knowledge of applicable regulatory guidelines (i.e. ICH and GCP) is strongly preferred
  • Possess a general understanding of clinical trial and drug development process, strong attention to detail, and meticulous follow-through
  • Provide high quality assistance supporting clinical trials according to applicable regulatory requirements and SOPs within budget and time lines
  • Communicate effectively with colleagues and vendors
  • Prepare, ship and manage inventory of study related supplies.
  • Assist in preparing materials for investigator and team meetings, study manuals etc.
  • Perform various job functions including but not limited to the following: tracking study specific documents, i.e. regulatory documents, enrollment and site activation, sample tracking, TMF maintenance, etc.
  • Contribute to the development of study specific tools
  • Coordinate and arrange meetings
  • Other duties and assignments as requested for the overall performance of the function and the company

Sthree US is acting as an Employment Business in relation to this vacancy.

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