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Contract CRA

  • Job type: Contract
  • Location: South San Francisco
  • Salary: Competitive
  • Job reference: SLHY
  • Sector: Clinical, EPM Scientific
  • Date posted: 28/11/2017
I currently have a role available as a CRA with a mid-size biotech company. The company is currently located in Redwood City, however, they will be moving to South San Fransisco in Q1 of 2018. Below is a brief overview of the role:
  • Biotech company focusing on oncology
  • 6-month contract with strong potential to extend
  • Phases 1-3
  • Currently located in Redwood City, relocating to South San Francisco 
  • Compensation is DOE
Responsibilities include: 
• Assists with developing clinical study protocols, case report forms, informed consent forms and other study-related documents

• Assists in study start-up, conduct, and close-out activities

• Acts as one of the primary contacts between the company and multiple clinical sites. Maintains close contact with sites by telephone, correspondence, and on-site visits

• Participates in investigator meetings

• Instructs investigators, study coordinators, and their personnel in regard to study protocol, regulatory requirements and conduct of the study

• Arranges for the availability of adequate study supplies

• Travels to clinical sites to monitor/co-monitor compliance with the study protocol, clinical trial material storage and accountability, GCP and FDA or other Health Authority regulations, and overall clinical objectives

• Verifies accuracy of clinical data through comparison of the case report forms to patient records at the site

• Approximately 30-40% yearly travel

• Interacts with personnel at Clinical Research Organizations as needed

If interested, please reach me at or (415)872-1747

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