Medpace Hiring Drug Safety Speialist in Pharmacovigilance Apply Now

About Company

Medpace is a full-service clinical contract research organization (CRO) providing 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 a 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, Medpace employs more than 5,000 people across 40+ countries.

Position Name : Drug Safety Specialist

Organization : Medpace

Qualification: B.Pharm, M.Pharm, Bsc, Msc, Pharm.D, Lifesciences, Nursing

Experience: 1 Year

Salary: ₹3L – ₹7L/yr

Location: Navi Mumbai

We are seeking a full-time, office-based Clinical Safety Coordinator to join our Clinical Safety department in India. This position involves handling and processing adverse events from all sources, including clinical trials and post-marketing surveillance. This role offers a fantastic opportunity to use your previous expertise and further develop your career.

Responsibilities:

Develop action plans for incoming safety-related calls.
Collect, process, and track adverse and serious adverse events.
Write detailed safety narratives.
Report 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, or Pharmacology.
Preferred: Clinical experience or experience in Clinical Research, case processing, and Post-Marketing Pharmacovigilance.
Proficient in English.
Strong knowledge of Microsoft® Office.
Broad knowledge of medical terminology.
Strong organizational and communication skills.