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Clinical Risk Management Associate


Please note that this is a 2 year contract assignment. Candidates cannot start an assignment until background check and drug test is completed
Qualifications:
Assists the CRMSS physician/management to: identify and clinically interprete safety signals; prepare responses to inquiries from health professionals and regulatory agencies regarding adverse experiences associated with Merck marketed products; perform safety surveillance review of serious adverse experience reports and other AE reports of interest to monitor and describe the safety profile of assigned products; and assist with the development and evaluation of pharmacovigilance and risk management plans.
Responsibilities:
Graduate degree in nursing, health sciences, pharmacology, epidemiology, public health, or other relevant health-related field. At least five years of experience in clinical, pharmacological, or related field of expertise. Excellent writing and communication skills a must. Experience in data analysis or the interpretation of adverse experience information is a plus.
Comments/Special Instructions
Candidate must have at least a Masters degree and have worked with patients in a medical or clinical setting as a Nurse, Pharmacist, etc

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