Clinical Safety Manager- Pharmacovigilance / Drug Safety Hiring at Medpace

Clinical Safety Manager- Pharmacovigilance / Drug Safety Hiring at Medpace

About the Role

Medpace is actively seeking a Clinical Safety Manager to join its Clinical Safety Department in Navi Mumbai, India. This full-time position is ideal for candidates with a strong background in pharmacovigilance, drug safety, and clinical research. As a pivotal role in the pharmacovigilance process, this position involves overseeing clinical safety case management, mentoring teams, and ensuring compliance with regulatory requirements.

If you have prior experience in clinical research and project management within pharmacovigilance and are eager to advance your career in a dynamic global CRO (Contract Research Organization), this is a great opportunity for you.

Key Responsibilities

• Lead and mentor a team of clinical safety professionals.
• Oversee case management and aggregate safety reporting to ensure high-quality client deliverables.
• Collaborate with clients and internal stakeholders, providing expert pharmacovigilance knowledge.
• Develop and implement safety management plans according to client requirements.
• Conduct safety reviews of clinical study documents, including protocols, study reports, and regulatory submissions.

Required Qualifications & Experience

• Education: Bachelor’s degree in a healthcare-related field (Pharmacy, Nursing, Pharmacology, or equivalent).
• Experience: At least 4 years of experience in clinical research or pharmacovigilance.
• Clinical Experience: A minimum of one year in clinical nursing is preferred.
• Project Management: Prior experience in project management is an added advantage.

Why Join Medpace?

Competitive Benefits & Growth Opportunities

• Flexible Work Environment: Work in a collaborative and innovative setting.
• Career Growth: Structured career paths with opportunities for professional development.
• Comprehensive Benefits: Competitive salary packages, PTO, and employee wellness initiatives.
• Global Impact: Work with a leading CRO that conducts Phase I-IV clinical trials across multiple therapeutic areas, including oncology, cardiology, and infectious diseases.

About Medpace

Medpace is a full-service clinical contract research organization (CRO) that partners with biotech, pharmaceutical, and medical device companies to accelerate drug development. With a presence in 40+ countries and a workforce of 5,000+ professionals, Medpace is a recognized leader in the industry.

Awards & Recognition

• Forbes: Named among America’s Most Successful Midsize Companies (2021-2024).
• Life Science Leader CRO Leadership Awards: Recognized for expertise, quality, reliability, and compatibility.

How to Apply?

Click here to apply: Medpace Careers

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