MDrug Safety Specialist Job in Navi Mumbai at Medpace. Apply online for clinical safety coordinator role with 1–3 years experience in pharmacovigilance.
If you are looking to build a career in pharmacovigilance and clinical research, this opportunity offers an excellent entry into global drug safety operations. A leading clinical research organization is hiring for Clinical Safety Coordinator roles, ideal for candidates with experience or interest in adverse event processing and clinical safety. This role provides exposure to international clinical trials and post-marketing surveillance activities.
Company Overview
Medpace Clinical Research India is part of a global full-service Contract Research Organization (CRO) headquartered in Cincinnati, USA. The company provides Phase I–IV clinical development services to pharmaceutical, biotechnology, and medical device industries. With a presence in over 40 countries and thousands of employees worldwide, Medpace is known for its scientific approach and commitment to advancing safe and effective therapies.
Job Overview (Job Details)
| Category | Details |
|---|---|
| Organization | Medpace Clinical Research India |
| Role | Drug Safety Specialist / Clinical Safety Coordinator |
| Qualification | Any Healthcare/Life Sciences Graduate |
| Experience | 1–3 Years |
| Job Location | Navi Mumbai |
| Employment Type | Full-Time (Office-based) |
| Application Mode | Online |
| Salary | Not Disclosed |
Job Location & Employment Type
The position is based in Navi Mumbai and requires candidates to work from the office. This is a full-time, permanent role within the Clinical Safety department.
Open Positions / Department Details
The hiring is for the Clinical Safety / Pharmacovigilance department. Selected candidates will work on adverse event handling and safety data processing related to clinical trials and post-marketing surveillance.
Key Roles & Responsibilities
Candidates selected for this role will be responsible for:
- Handling incoming adverse event reports from multiple sources
- Processing and tracking adverse events (AEs) and serious adverse events (SAEs)
- Writing detailed safety narratives
- Managing and reporting safety data accurately
- Coordinating with internal teams and clinical research sites
- Ensuring compliance with pharmacovigilance and clinical safety processes
- Supporting safety data management and documentation
Eligibility Criteria
Education
- Bachelor’s degree in a healthcare or life sciences field
(Pharmacy, Nursing, Pharmacology, or related disciplines)
Experience
- 1–3 years of experience preferred
- Experience in clinical research, pharmacovigilance, or case processing is an advantage
Skills Required
- Good knowledge of medical terminology
- Strong communication skills in English
- Proficiency in Microsoft Office tools
- Attention to detail and organizational skills
- Ability to manage multiple tasks and timelines
- Understanding of pharmacovigilance and clinical safety concepts
Salary & Benefits
- Salary: Not disclosed by the company
- Flexible work environment
- Competitive compensation and benefits package
- Paid time off (PTO) and employee wellness initiatives
- Structured career growth and learning opportunities
- Exposure to global clinical trials and safety operations
Selection Process
The hiring process typically includes:
- Online Application
- Resume Screening
- Technical/Functional Interview
- HR Discussion
- Final Selection
Shortlisted candidates will be contacted by the recruitment team for further steps.
How to Apply
Interested candidates can apply through the official online application portal of the company. Ensure your resume highlights your experience in pharmacovigilance, clinical research, or safety data handling.
Important Dates
- Application Deadline: Not specified (apply as early as possible)
Why Apply for This Pharma Job?
This role offers an excellent opportunity to work with a globally recognized CRO and gain exposure to international clinical safety standards. Candidates will develop expertise in adverse event processing, safety narratives, and regulatory compliance.
Working in clinical safety opens doors to long-term careers in pharmacovigilance, drug safety, and regulatory affairs. The structured growth path and global exposure make this role highly valuable for career advancement.
Important Note / Disclaimer
IndiaPharmaJobs.in is an independent job information platform and is not affiliated with any recruiter or company. We do not charge any fee for job applications. Candidates are advised to verify all details independently before applying.
Final Call-to-Action
If you are looking to build a career in pharmacovigilance and clinical research, this is a great opportunity. Apply now and take the next step toward a global career in drug safety.
