Covance Clinical Research Associate II (1 year contract) in Vietnam
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
Bachelor of health sciences, nursing, biomedical sciences, pharmacy, pharmacology, or a related discipline.
Ability to work independently, coupled with management and organizational skills.
• Understanding of the regulatory context, good clinical practices and standard
• Availability to travel frequently.
At least one year CRA experience
Job Number 2018-19795
Job Category Clinical Research Associate
Position Type Hidden (2052)
Covance is committed to diversity in the workplace and is an equal opportunity employer (Minority/Female/Individual with Disability/Veteran/Sexual Orientation/Gender Identity). Your confidentiality and privacy are important to us.