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Position: Drug Safety Specialist
- Position Name: Drug Safety Specialist
- Company Name: Medpace
- Department: Clinical Safety
- Qualification: B.Pharm, M.Pharm, Pharm.D, M.Sc, B.Sc, Life Sciences
- Experience: 1 to 2 Years
- Job Location: Mumbai
- Website: Wikipedia page on pharmacovigilance
About Medpace
Medpace is a leading full-service clinical contract research organization (CRO) dedicated to accelerating the global development of safe and effective medical therapeutics. With over 30 years of experience and a presence in over 40 countries, we specialize in clinical development services for the biotechnology, pharmaceutical, and medical device industries. Our mission is to advance the field of clinical research through a disciplined and scientific approach.
Job Summary
We are seeking a full-time, office-based Drug Safety Specialist to join our Clinical Safety department in Mumbai. This role focuses on managing and processing adverse events from various sources, including clinical trials and post-marketing surveillance.
If you are passionate about pharmacovigilance and want to advance your career in a dynamic environment, this opportunity is for you!
Key Responsibilities
As a Drug Safety Specialist at Medpace, you will:
- 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.
For more information, visit the Wikipedia page on pharmacovigilance.
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.
Apply Now to join Medpace and contribute to cutting-edge clinical research that transforms lives!
Feel free to modify or request further adjustments as needed!
