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Clinical Safety Manager- Pharmacovigilance / Drug Safety

Medpace
Medpace
4+ years
Not Disclosed
10 Jan. 31, 2025
Job Description
Job Type: Full Time Education: B.Sc./M.Sc./B.Pharm/M.Pharm/Life science Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

📌 Clinical Safety Manager - Pharmacovigilance / Drug Safety | Medpace
📍 Location: Navi Mumbai, India
🚀 Join a Leading Clinical Research Organization

🌟 About Medpace

Medpace is a full-service contract research organization (CRO) providing clinical development services to the biotech, pharmaceutical, and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics, positively impacting patients' lives worldwide.

📝 About the Role

We are seeking a Clinical Safety Manager to join our Clinical Safety Department in India. This full-time position plays a pivotal role in pharmacovigilance at Medpace, offering the opportunity to leverage your nursing or pharmacovigilance expertise while advancing your career.

🔍 Key Responsibilities

Team Leadership: Line manage, mentor, and develop a team of clinical safety professionals.
Client & Stakeholder Management: Provide expert safety knowledge while managing relationships with clients and internal stakeholders.
Safety Case Management: Oversee clinical safety case management and aggregate reporting to meet client needs.
Safety Review: Review clinical study documents (e.g., protocols, study reports) and marketing application components.
Safety Plans: Create customized safety management plans tailored to clients' needs.

📋 Qualifications

🎓 Bachelor's degree in Healthcare-related field (e.g., Nursing, Pharmacy, Pharmacology).
📌 At least 4 years of clinical research/pharmacovigilance experience.
📌 At least 1 year of clinical nursing experience.
📌 Prior project management experience preferred.

💼 Why Join Medpace?

🌏 Global Impact: Join a team working toward improving lives globally.
📈 Career Development: Structured paths for professional growth and leadership opportunities.
🎉 Employee Perks: Flexible work, competitive compensation, health/wellness initiatives, and company-sponsored appreciation events.

🏆 Medpace Accolades

🏅 Forbes Recognition: One of America's Most Successful Midsize Companies (2021-2024).
🏅 CRO Leadership Awards: Recognized for expertise, quality, capabilities, and reliability.

📩 Apply Now