Covance
Clinical Research Associate
Job
Overview:
Monitor
multiple Phase I, II, III & IV clinical trial sites, across therapeutic
areas. Assist other CRA with co-monitoring activities both remote and on-site
as needed.
Target
5-10 site assignments (depending on complexity/enrollment/stage of study),
average 2-3 protocols and 1-2 therapeutic areas at any given time. The number
would be adjusted based on the workload assignment.
Education/Qualifications:
Must
have a Bachelor's Degree (or equivalent).
Experience:
2 -
4 years of relevant healthcare experience in the pharmaceutical industry or
clinical research, including minimum 6-12 months of monitoring and site
management experience.
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