Senior Clinical Research Associate At Everest
Job Description & How to Apply Below
Responsibilities Interact with study Sponsors and investigational sites
Perform site feasibility and pre-study visits
Conduct interim and close-out monitoring visits
Review and submit quality monitoring visit reports
Assist with training sessions for site personnel
Qualifications Bachelor’s degree in Life Sciences
Minimum of 4 years' clinical trial monitoring experience
In-depth knowledge of ICH-GCP guidelines
Experience in Pain, Oncology, and CNS areas
Excellent communication skills and organizational abilities
Drive quality clinical research and ensure compliance as part of the Everest team.
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Position Requirements
10+ Years
work experience
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