Medpace is seeking a motivated individual to join the Clinical Safety team in Stirling. This role involves critical tasks in pharmacovigilance, including collecting safety reports, generating necessary documents, and ensuring compliance with clinical trial standards.
Ideal candidates should possess at least 2 years of experience in clinical trial pharmacovigilance, a Bachelor’s degree in a life science, and familiarity with safety databases such as Argus. Medpace offers a flexible work environment and competitive benefits.
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