Covance Clinical Research Associate II (1 year contract) in Vietnam

Job Overview

  • Responsible for all aspects of study site monitoring including routine monitoring and close-out of clinical site, maintenance of study files, conduct of pre-study and initiation visit, with or without guidance, liaise with vendors and other duties as assigned

  • Assist with the administration of clinical research projects, recruiting investigators and collect investigator documentation and site management

  • Provide coverage for clinical contact telephone lines, as required

  • Update, track and maintain study-specific trial management tools/systems

  • Generate and track drug shipments and supplies, as needed

  • Implement study specific communication plan as assigned

  • Assist Senior CRA in managing investigator site budgets

  • Perform other duties as assigned by management

Education/Qualifications

  • Bachelor of health sciences, nursing, biomedical sciences, pharmacy, pharmacology, or a related discipline.

  • Ability to work independently, coupled with management and organizational skills.

  • Good English

• Understanding of the regulatory context, good clinical practices and standard

operating procedures.

• Availability to travel frequently.

Experience

At least one year CRA experience

Job Number 2018-19795

Job Category Clinical Research Associate

Position Type Hidden (2052)

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