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    Medpace Hiring Drug Safety Specialist | Pharmacovigilance Job Opportunity | B Pharm Graduates | Apply Now

    Pharmacovigilance Job at MedPace Careers | Drug Safety Specialist Role | Apply Now

    Searching for a rewarding Pharmacovigilance Job with leading global CROs? Medpace is offering excellent Medpace Careers opportunities for the role of Drug Safety Specialist/Clinical Safety Coordinator in Navi Mumbai. Candidates with backgrounds in Pharmacy, Pharmacology, Nursing, or Clinical Research can apply for this exciting role focused on adverse event processing, clinical safety operations, and post-marketing surveillance. This opportunity is ideal for professionals looking to build long-term careers in pharmacovigilance and clinical research.

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

    About the Company

    Medpace is a full-service clinical contract research organization (CRO) providing Phase I-IV clinical development services to biotechnology, pharmaceutical, and medical device industries. Through expanding Medpace Careers, the company focuses on accelerating the development of safe and effective therapeutics globally. Headquartered in Cincinnati, Ohio, Medpace employs more than 6,000 professionals across 40+ countries.

    Job Description

    Medpace is currently seeking a full-time, office-based Clinical Safety Coordinator to join its Clinical Safety department in India. This Pharmacovigilance Job under Medpace Careers will focus on handling and processing adverse events from multiple sources, including clinical trials and post-marketing surveillance.

    Candidates interested in drug safety, case processing, and clinical research operations can benefit from this excellent career opportunity.

    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 such as Nursing, Pharmacy, Pharmacology, etc.
    • Clinical experience or Clinical Research, case processing, and post-marketing Pharmacovigilance experience preferred
    • Proficient English communication skills required
    • Proficient knowledge of Microsoft Office
    • Broad knowledge of medical terminology
    • Strong organizational and communication skills

    Employee Benefits

    • Flexible work environment
    • Competitive compensation and benefits package
    • Competitive PTO packages
    • Structured career development opportunities
    • Company-sponsored employee appreciation events
    • Employee health and wellness initiatives

    CLICK HERE TO APPLY ONLINE

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