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    Pharmacy Job at Medpace | Apply Now for the Drug Safety Specialist Role

    Pharmacy Job at Medpace | Apply Now for the Drug Safety Specialist Role

    Medpace, a globally recognized full-service CRO, is seeking a Drug Safety Specialist / Clinical Safety Coordinator to join its Clinical Safety team in Navi Mumbai, India. This Pharmacy Job focuses on the critical handling and processing of adverse events originating from both clinical trials and post-marketing surveillance. We highly encourage Nursing Professionals, Pharmacists, and candidates with a Bachelor’s degree in a Healthcare-related field and relevant experience in Pharmacovigilance (PV) or clinical research, looking for structured career growth, to apply.

    • Position: Drug Safety Specialist/ Clinical Safety Coordinator 
    • Location: Navi Mumbai, India
    • Job ID: 10603

    About The Company

    Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries.

    Job Summary

    We are currently seeking a full-time, office-based Clinical Safety Coordinator to join our Clinical Safety department in India. This position will be focused on the handling and processing of adverse events from all sources, including clinical trials and post marketing surveillance.

    If you want an exciting career where you use your previous expertise and can develop and grow your career even further, then this is the opportunity for you!

    Responsibilities of the Pharmacology Job

    • Determine plan of action for incoming calls;
    • Collect, process, and track incoming adverse and serious adverse events;
    • Write safety narratives;
    • Report on various safety data; and
    • Collaborate with internal departments and investigative clinical research sites to ensure compliance with safety processes.

    Qualifications required for the Pharmacology Job

    • Bachelor’s degree in  Pharmacy, Pharmacology, etc
    • Clinical experience or Clinical Research, case processing and Post marketing Pharmacovigilance experience is preferred;
    • Proficient English is required
    • Proficient knowledge of Microsoft® Office;
    • Broad knowledge of medical terminology; and
    • Strong organizational and communication skills.

    Why Medpace?

    People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today.

    The work we’ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future.

    APPLY ONLINE HERE

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