Medpace, a leading full-service clinical contract research organization (CRO), is seeking a full-time, office-based Drug Safety Specialist to join our Clinical Safety department in Mumbai. With over 30 years of experience and a global presence in more than 40 countries, Medpace is dedicated to advancing the field of clinical research and ensuring the safety and efficacy of medical therapeutics.

Job Overview

Position: Drug Safety Specialist

Company Profile: Medpace is committed to providing comprehensive clinical development services for the biotechnology, pharmaceutical, and medical device industries. Our mission is to improve healthcare outcomes through a disciplined, scientific approach to clinical research.

Vacancy Details

Organization:	Medpace
Position:	Drug Safety Specialist
Qualification:	B.Pharm, M.Pharm, Pharm.D, M.Sc, B.Sc, Life Sciences
Experience:	1 to 2 Years of experience in clinical research, case processing, or post-marketing pharmacovigilance.
Job Location:	Mumbai, Maharashtra

Job Summary

We are looking for a Drug Safety Specialist who will be responsible for managing and processing adverse events from various sources, including clinical trials and post-marketing surveillance. The ideal candidate will have a strong background in pharmacovigilance, clinical research, or a related field, with excellent organizational and communication skills.

Key Responsibilities

• Determine Plan of Action: Develop strategies for handling incoming calls related to drug safety.
• Collect and Process Data: Track and process incoming adverse and serious adverse events.
• Write Safety Narratives: Document and report on safety data and events.
• Ensure Compliance: Collaborate with internal departments and clinical research sites to uphold safety processes.

Qualifications

Required:

• Education: Bachelor’s degree in a healthcare-related field such as Nursing, Pharmacy, Pharmacology, etc.
• Experience: 1 to 2 years in clinical research, case processing, or post-marketing pharmacovigilance.
• Skills: Proficiency in English, Microsoft® Office, and a broad knowledge of medical terminology.
• Communication: Strong organizational and communication skills.

Preferred:

• Clinical experience or previous experience in pharmacovigilance.

Medpace Overview

Medpace offers a range of services including Phase I-IV clinical development, with expertise in various therapeutic areas such as oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral, and anti-infective. Our work has a significant impact on the lives of patients and families across the globe.

Why Medpace?

At Medpace, we are driven by our commitment to making a difference. Our work has a significant impact on the lives of patients and families across the globe. By joining us, you become part of a dedicated team that strives to improve healthcare outcomes through innovative research.

Medpace Perks

• Hybrid Work Options: Flexible work-from-home opportunities based on position and level.
• Competitive PTO: Generous paid time off packages.
• Employee Events: Company-sponsored appreciation events.
• Health and Wellness: Initiatives to support employee well-being.
• Flexible Schedule: Options for flexible work hours.
• Competitive Compensation: Attractive salary and benefits package.
• Career Growth: Structured paths for professional development.

How to Apply

Ready to join the Medpace team and contribute to cutting-edge clinical research that transforms lives? Apply now to take the next step in your career as a Drug Safety Specialist at Medpace!

Apply Now

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