Global Studies Associate

South San Francisco, CA 94080 | Contract

Post Date: 06/11/2018 Job ID: 4362 Industry: Drug Development - Med/Clinical Affairs

Our client is a leading biotechnology company that discovers, develops, manufactures and commercializes medicines to treat patients with serious or life-threatening medical conditions. They are among the world' s leading biotech companies, with multiple products on the market and a promising development pipeline.

 

Duties:
  • Main Responsibilities and Accountabilities:
    • Develops and maintains effective working relationships with members of the SMT involved in running clinical studies
    • Assists the GSM with effective communication and information sharing within the SMT and with external partners
    • General project support
    • Provides the SMT with guidance and know how to support the effective use of system functionality and reports to ensure consistency across SMTs
    • Work in both US & ex-US in-sourced (CCO) & outsourced (CRO) study teams Distinguishing requirements of the role:
    • Comfortable working across different cultures & time zones, and with internal & CRO / vendor colleagues
    • High level of proficiency in written & oral communication abilities
    • Will be assigned  5 clinical trials
    • Works with study vendors & systems expert
    • Prioritizes and multitasks to ensure that tasks are completed on time
    • Self-motivated and displays initiative (resourceful) - for instance to move actions forward without the need for continual supervision

 

 

Skills:

  • Willingness to Work on Site Mon-Fri, 8 hr days; remote working opportunity may be considered per department policy
  • Flexibility to participate in early morning TCs. Hit the ground running;
  • Perform duties with little oversight from manager Willingness to complete on-line & instructor-led training: SOP / Healthcare Compliance

 

Education:

  • Bachelors
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