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Full Job Description
Job Summary
Our clinical operations activities are growing rapidly, and we are currently seeking a full-time, Clinical Safety Manager to join our Clinical Safety Department. This position plays a key role in the pharmacovigilance process at Medpace. If you want an exciting career where you use your previous nursing or pharmacovigilance expertise and can develop and grow your career even further, then this is the opportunity for you.
Responsibilities
Line manage, mentor and develop a team of clinical safety professionals;
Manage relationships with clients and internal stakeholders by providing expert safety knowledge;
Oversee clinical safety case management and aggregate reporting responsibilities of direct reports to ensure client needs are fulfilled to high quality;
Create safety management plans dependent upon client;
Provide safety review of clinical study documents, including protocols, study reports; and marketing application components
Qualifications
BSN or equivalent healthcare experience with a bachelor's degree;
At least 4 years of clinical research/pharmacovigilance experience;
Ideally one year of clinical nursing experience; and
Prior project management experience is preferred.
What to Expect Next
A Medpace team member will review your application and if your profile matches our current needs, you will be contacted for an interview. While we review all applications carefully, we are unable to respond to every applicant, and only candidates selected for interviews will be contacted.
About Medpace
Medpace is a clinical research organization that provides services to pharmaceutical, biotechnology, and medical device companies. The company's services include clinical trial management, regulatory consulting, and medical imaging. Medpace was founded in 1992 and is headquartered in Cincinnati, Ohio. The company has operations in North America, Europe, and Asia.
