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Drug Safety Specialist Hiring at Medpace | Mumbai

ByPharma Hiring Hub

Medpace is hiring for the role of Drug Safety Specialist (Clinical Safety Coordinator) at its Navi Mumbai office. This full‑time, office‑based opportunity is ideal for professionals with 1 to 3 years of experience in pharmacovigilance, clinical safety, or drug safety operations. The role focuses on adverse event (AE) and serious adverse event (SAE) processing across clinical trials and post‑marketing surveillance activities, offering strong exposure to global clinical safety operations.

Medpace

🏢 Company Overview

Medpace is a global, full‑service Contract Research Organization (CRO) that supports pharmaceutical, biotechnology, and medical device companies through all phases of clinical research. Known for its scientific expertise and strong internal training culture, Medpace provides a structured environment where professionals can develop deep expertise in clinical safety, regulatory compliance, and global pharmacovigilance operations.

📊 Internship Overview

  • Company Name: Medpace
  • Job Role: Drug Safety Specialist / Clinical Safety Coordinator
  • Employment Type: Full‑Time (Office‑based)
  • Experience Required: 1 to 3 Years
  • Functional Area: Pharmacovigilance / Clinical Safety
  • Job Location: Navi Mumbai

📋 What You Will Do

  • Determining appropriate actions for incoming safety‑related calls
  • Collecting, processing, and tracking adverse events (AEs) and serious adverse events (SAEs)
  • Writing clear and accurate safety narratives
  • Supporting safety data reporting and documentation activities
  • Reviewing and maintaining safety information within tracking systems
  • Collaborating with internal departments to ensure safety workflows are followed
  • Coordinating with investigative clinical research sites to ensure compliance with safety reporting requirements
  • Supporting ongoing clinical trials and post‑marketing surveillance activities

🎓 Who Can Apply

  • Candidates applying for this role should meet the following criteria:
  • Educational Background:
    • Bachelor’s degree in a healthcare‑related field, such as:
      • Nursing
      • Pharmacy
      • Pharmacology
      • Or related disciplines
  • Experience:
  • 1 to 3 years of experience in:
    • Pharmacovigilance
    • Clinical safety
    • Case processing
    • Post‑marketing drug safety or clinical research (preferred)

🧠 Required Skills

The following skills are essential for success in this role:

  • Strong knowledge of medical terminology
  • Proficiency in English (written and verbal)
  • Good working knowledge of Microsoft Office applications
  • Strong organizational and time‑management skills
  • Excellent communication and interpersonal skills
  • Ability to work accurately and manage multiple safety cases

⭐ Role Insight

The Drug Safety Specialist role at Medpace offers hands‑on involvement in end‑to‑end adverse event processing across both clinical trial and post‑marketing environments. Professionals in this role play a critical part in ensuring patient safety and regulatory compliance. Working at Medpace provides structured learning, strong mentorship, and opportunities to grow into senior safety, management, or regulatory roles.

🎯 Suitable For

This Opportunity is ideal for:

  • Pharmacovigilance professionals with 1–3 years of experience
  • Candidates with hands‑on AE/SAE processing exposure
  • Clinical research professionals transitioning into drug safety roles
  • Individuals seeking a long‑term career in clinical safety operations

🎁 Medpace Perks & Benefits

Medpace offers a supportive and employee‑focused work environment, including:

  • Flexible and supportive work culture
  • Competitive compensation and benefits package
  • Generous paid time‑off (PTO) packages
  • Structured career paths with clear progression opportunities
  • Company‑sponsored employee appreciation events
  • Employee health and wellness initiatives

📈Growth Opportunities

With experience and performance, Drug Safety Specialists at Medpace can progress into roles such as:

  • Senior Drug Safety Specialist
  • Clinical Safety Scientist
  • Safety Team Lead
  • Pharmacovigilance Manager

🔗 How To apply

Interested candidates should apply only through the official company career website using the link provided below.

Application Link

Important Disclaimer: This job post is shared for informational purposes only, based on publicly available job details. Candidates are advised to verify eligibility, job responsibilities, and application procedures from the official website before applying.

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❓ Frequently Asked Questions (FAQs)

1.Which safety databases are commonly used in this role?

You may work with global safety databases such as Argus, ArisG, or similar systems used across Medpace’s global projects.

2. Does the role involve regulatory submissions?

Yes. You will support timely safety reporting and regulatory submissions according to global regulations and client SOPs.

3.What skills are most important for success in this role?

Strong medical terminology knowledge
Attention to detail and accuracy
Ability to follow SOP‑driven processes
Time management and multitasking
Clear written and verbal communication
Quality and compliance mindset

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