Medpace is hiring a Clinical Safety Coordinator for its Navi Mumbai office. This is a great opportunity for professionals with clinical research or pharmacovigilance background seeking pharma jobs, QA jobs, and pharmaceutical careers in India in drug safety and clinical development.
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About the Company
Medpace is a full-service global clinical contract research organization (CRO) providing Phase I-IV clinical development services to biotechnology, pharmaceutical, and medical device companies. Headquartered in Cincinnati, Ohio, Medpace operates across 40+ countries with over 6,000 employees. The company is recognized for its scientific excellence, disciplined approach, and strong regulatory compliance.
It has earned multiple CRO Leadership Awards and is consistently ranked among America’s most successful midsize companies by Forbes. Medpace focuses on therapeutic areas including oncology, cardiology, CNS, and anti-infectives.
Job Details
- Company Name: Medpace
- Experience: Clinical Research / Pharmacovigilance experience preferred
- Qualification: Bachelor’s degree in Healthcare-related field (Nursing, Pharmacy, Pharmacology, etc.)
- Location: Navi Mumbai, India
- Work Type: On-site (Office-based)
Job Description
Medpace is looking for a full-time Clinical Safety Coordinator to join the Clinical Safety department in Navi Mumbai. This role focuses on processing adverse events from clinical trials and post-marketing surveillance, ensuring high standards of drug safety and regulatory compliance in global clinical development programs.
Clinical Safety Coordinator / Drug Safety Specialist
- Department: Clinical Safety
- Role: Adverse event processing and safety management
- Experience: Preferred clinical research or pharmacovigilance background Education/Qualification: Bachelor’s degree in Healthcare-related field (Nursing, Pharmacy, Pharmacology, etc.)
Skills/Qualifications
- Bachelor’s degree in Nursing, Pharmacy, Pharmacology, or related healthcare field
- Clinical experience or Clinical Research background preferred
- Case processing and Post-marketing Pharmacovigilance experience preferred
- Proficient in English language (written and spoken)
- Strong knowledge of medical terminology
- Excellent organizational and communication skills
- Proficient in Microsoft Office applications
Key Responsibilities
- Handle incoming safety-related calls and determine action plans
- Collect, process, and track adverse and serious adverse events
- Write detailed safety narratives
- Report on various safety data
- Collaborate with internal teams and clinical research sites
- Ensure compliance with safety reporting processes
- Support timely and accurate safety documentation
Benefits/Perks
- Competitive compensation and benefits package
- Flexible work environment
- Structured career paths with professional growth opportunities
- Generous PTO packages
- Employee health and wellness initiatives
- Company-sponsored appreciation events
- Global exposure in clinical research projects
For more pharma jobs and CRO opportunities across India, visit Pharma Recruiter.
How to Apply
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Verification: To confirm the legitimacy of this posting, you can view the original announcement on the Medpace career page.
🔗 Click below to apply directly for this job
Interested candidates can apply directly through Medpace’s career portal at Medpace.com. Submit your updated resume highlighting relevant clinical or pharmacovigilance experience. A Medpace team member will review your application and contact shortlisted candidates for the next steps.
Apply now and take your career in drug safety to the next level with Medpace!
Why You Should Join Medpace
Medpace offers a dynamic culture driven by People, Purpose, and Passion. Employees enjoy long-term career stability, continuous learning, and recognition for their contributions to global clinical trials. Working here means being part of an innovative, compliant, and high-performing environment that accelerates the development of safe and effective medical treatments worldwide.
FAQs
Q1: What qualification is required for the Clinical Safety Coordinator role?
A: A Bachelor’s degree in a healthcare-related field such as Nursing, Pharmacy, or Pharmacology is required.
Q2: Is prior experience mandatory for this Medpace pharma job?
A: Clinical research, case processing, or post-marketing pharmacovigilance experience is preferred but not strictly mandatory.
Q3: What is the work location for this position?
A: The role is office-based in Navi Mumbai, Maharashtra.
Q4: What growth opportunities does Medpace offer?
A: The company provides structured career progression, global project exposure, and professional development in clinical safety and pharmacovigilance.
