Drug Safety Specialist/Clinical Safety Coordinator Vacancy at Medpace

Drug Safety Specialist/Clinical Safety Coordinator – Navi Mumbai, 2025

Apply for Drug Safety Specialist/Clinical Safety Coordinator at Medpace, Navi Mumbai. Bachelor’s degree required. 2025 vacancies open.

Medpace, a globally recognized full-service Clinical Research Organization (CRO), is inviting applications for the role of Drug Safety Specialist/Clinical Safety Coordinator in Navi Mumbai, India. This position provides an exciting opportunity to contribute to clinical safety, pharmacovigilance, and post-marketing surveillance while building a rewarding career in clinical research.

Company Overview

Medpace is a leading clinical CRO providing Phase I-IV development services to the biotechnology, pharmaceutical, and medical device industries. Headquartered in Cincinnati, Ohio, with over 5,000 employees across 40+ countries, Medpace leverages local regulatory and therapeutic expertise in oncology, cardiology, metabolic disease, endocrinology, CNS, anti-viral, and anti-infective areas. The company emphasizes scientific rigor, discipline, and a mission to accelerate the global development of safe and effective medical therapeutics.

Why Work at Medpace?

• People, Purpose, Passion: Join a team dedicated to making a difference in patient lives worldwide.
• Impactful Work: Contribute to advancing therapies across multiple therapeutic areas.
• Recognition & Awards: Forbes-recognized for midsize company excellence; multiple CRO leadership awards.
• Career Growth: Structured career paths, employee appreciation events, health and wellness initiatives.
• Flexible Work Environment: Encouraging work-life balance and professional development.

Job Role & Responsibilities

As a Drug Safety Specialist/Clinical Safety Coordinator, you will play a critical role in handling adverse events, supporting pharmacovigilance activities, and ensuring compliance with clinical safety processes. Key responsibilities include:

• Determining the appropriate plan of action for incoming calls regarding adverse events.
• Collecting, processing, and tracking incoming adverse and serious adverse events from clinical trials and post-marketing surveillance.
• Writing clear and comprehensive safety narratives.
• Reporting and analyzing safety data to ensure timely regulatory submission.
• Collaborating with internal departments and investigative clinical research sites to maintain compliance with safety processes.

Eligibility / Qualifications

• Education: Bachelor’s degree in Healthcare-related fields such as Nursing, Pharmacy, Pharmacology, or related disciplines.
• Experience: Clinical experience, clinical research, case processing, and post-marketing pharmacovigilance preferred.
• Skills:
  • Proficient English communication (written and verbal)
  • Strong knowledge of medical terminology
  • Proficiency in Microsoft Office Suite
  • Strong organizational, analytical, and communication skills

Relevant Courses: B.Pharm, M.Pharm, Pharm.D, Nursing, Clinical Research, Biotechnology, Life Sciences.

Location & Salary

• Location: Navi Mumbai, Maharashtra, India (Office-based)
• Salary: Competitive, commensurate with qualifications and experience. Additional benefits include flexible work arrangements, health initiatives, and PTO packages.

Application Process

Interested candidates can apply online via Medpace’s official careers portal: Apply Here. Ensure your resume highlights relevant education, skills, and pharmacovigilance experience to enhance your chances. Apply promptly to secure your opportunity!

FAQs

Q1: Can freshers apply for this role?
A1: Freshers with relevant healthcare education and interest in pharmacovigilance may apply, though prior clinical experience is preferred.

Q2: What is the required qualification?
A2: Bachelor’s degree in Nursing, Pharmacy, Pharmacology, or related healthcare fields.

Q3: Is this a remote position?
A3: No, the role is office-based in Navi Mumbai.

Q4: What skills are necessary?
A4: Strong communication, medical terminology knowledge, Microsoft Office proficiency, and attention to detail.

Q5: How many vacancies are open?
A5: Multiple vacancies (2025) are currently open for eligible candidates.

Why This Role Matters

Joining Medpace as a Drug Safety Specialist/Clinical Safety Coordinator provides an impactful career path in clinical research and pharmacovigilance. You will contribute directly to patient safety, regulatory compliance, and the advancement of medical therapeutics globally. The role ensures continuous professional development while making a meaningful difference in healthcare outcomes.

Take the first step toward a rewarding pharmacovigilance career—apply today!

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