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    Medpace Hiring Drug Safety Specialists | Pharmacy Graduates Eligible

    Pharmacovigilance Job at Medpace | Excellent Opportunity for B.Pharm & M.Pharm

    Looking for a Pharmacovigilance Job in India? Medpace Careers is hiring for the position of Drug Safety Specialist / Clinical Safety Coordinator in Navi Mumbai. This exciting opportunity is ideal for Pharmacy graduates who want to build a successful career in Pharmacovigilance, Clinical Safety, and Clinical Research. If you’re seeking a rewarding Pharmacovigilance Job, don’t miss this excellent opportunity with Medpace Careers.

    • Job Title: Drug Safety Specialist/Clinical Safety Coordinator
    • Location: Navi Mumbai, India
    • Department: Clinical Safety
    • Job ID: 11946

    About the Company

    Medpace Careers offers exciting opportunities for professionals looking to grow in Clinical Research and Pharmacovigilance. Medpace is a global Contract Research Organization (CRO) providing comprehensive Phase I–IV clinical development services to the biotechnology, pharmaceutical, and medical device industries.

    Headquartered in Cincinnati, Ohio, Medpace has more than 6,000 employees across 40+ countries, supporting therapeutic areas including Oncology, Cardiology, Metabolic Diseases, Endocrinology, Central Nervous System, Anti-Viral, and Anti-Infective research.

    Job Description

    Medpace Careers is currently seeking a full-time, office-based Drug Safety Specialist / Clinical Safety Coordinator to join its Clinical Safety department in Navi Mumbai.

    This Pharmacovigilance Job focuses on handling and processing adverse events from various sources, including clinical trials and post-marketing surveillance. It is an excellent opportunity for candidates who want to build expertise in Drug Safety, Case Processing, and Clinical Safety.

    Key Responsibilities

    • 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;
    • Collaborate with internal departments and investigative clinical research sites to ensure compliance with safety processes.

    Qualifications

    • Bachelor’s degree in a healthcare-related field (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 Join Medpace Careers?

    • Global career opportunities in Pharmacovigilance and Clinical Safety.
    • Exposure to international clinical trials and post-marketing safety activities.
    • Career development with one of the world’s leading CROs.
    • Collaborative work environment.
    • Opportunities to enhance your expertise in Drug Safety and Clinical Research

    CLICK HERE TO APPLY ONLINE

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