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Sr. Clinical Research Associate, IQVIA
Lifelancer
Bloomington, IN
Category
Consulting
Apply for Job
Job Description
Perform site monitoring visits, adapt, drive, and track subject recruitment plans, administer protocol and related study training, and evaluate site practices in accordance with contracted scope of work and Good Clinical Practice.
Requirements
Bachelor's Degree in scientific discipline or health care
At least 2 years of on-site monitoring experience
Good knowledge of clinical research regulatory requirements and Good Clinical Practice (GCP) guidelines
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