Medpace Hiring for Safety Database Specialist, Drug Safety Specialist & Project Coordinator Roles
Global CRO company Medpace has announced multiple hiring opportunities for candidates in Clinical Safety, Pharmacovigilance, Safety Database Management, and Core Laboratory Project Coordination across Navi Mumbai and Hyderabad locations.
These openings are ideal for life sciences, pharmacy, biomedical engineering, and healthcare graduates looking to build careers in clinical research and the pharmaceutical industry.
Medpace is actively recruiting for Safety Database Specialist, Drug Safety Specialist / Clinical Safety Coordinator, and Project Coordinator roles across multiple departments in India.
📋 Available Job Openings at Medpace India 2026
| Role | Location | Department |
|---|---|---|
| Safety Database Specialist | Navi Mumbai | Clinical Safety |
| Drug Safety Specialist / Clinical Safety Coordinator | Navi Mumbai | Clinical Safety |
| Project Coordinator – Core Laboratory | Hyderabad | Imaging Services |
| Project Coordinator – Core Laboratory | Navi Mumbai | Imaging Services |
💊 1. Safety Database Specialist – Navi Mumbai
| Details | Information |
|---|---|
| Department | Clinical Safety |
| Location | Navi Mumbai |
| Job ID | 11954 |
| Experience | 1–2 Years |
| Qualification | Scientific Discipline / Business Informatics |
📌 Key Responsibilities
- Configure products, studies, and licenses in Argus and Argus J.
- Support Oracle Business Intelligence (OBIEE) reporting.
- Resolve safety database-related issues.
- Execute User Acceptance Testing (UAT).
- Generate outputs for DSUR, PSUR, and PBRER reports.
- Support audits, inspections, SOPs, and training activities.
🎓 Required Qualifications
- Bachelor’s degree in scientific discipline or Business Informatics.
- 1–2 years of related experience.
- Experience with Argus Safety Database and SQL preferred.
- Knowledge of OBIEE reporting tools.
- Strong analytical and problem-solving skills.
💡 Preferred Skills
- Pharmacovigilance systems experience.
- CRO or pharmaceutical industry background.
- Study configuration expertise in safety systems.
💉 2. Drug Safety Specialist / Clinical Safety Coordinator – Navi Mumbai
| Details | Information |
|---|---|
| Department | Clinical Safety |
| Location | Navi Mumbai |
| Job ID | 11946 |
| Qualification | Pharmacy, Nursing, Pharmacology, Healthcare |
| Experience | 0–4 Years |
📌 Key Responsibilities
- Process adverse event and serious adverse event cases.
- Write medical safety narratives.
- Track and manage pharmacovigilance reports.
- Collaborate with clinical research sites and internal teams.
- Maintain compliance with global safety processes.
🎓 Required Qualifications
- Bachelor’s degree in Pharmacy, Nursing, Pharmacology, or Healthcare.
- Knowledge of medical terminology.
- Good communication and organizational skills.
- Pharmacovigilance or case processing experience preferred.
- Microsoft Office proficiency required.
🧪 3. Project Coordinator – Core Laboratory (Hyderabad)
| Details | Information |
|---|---|
| Department | Imaging Services |
| Location | Hyderabad |
| Job ID | 11936 |
| Qualification | Biomedical Engineering |
| Experience | Research Experience Preferred |
📌 Responsibilities
- Maintain imaging study timelines and reports.
- Manage imaging supply inventory for study sites.
- Coordinate with internal teams and research sites.
- Support imaging and core laboratory operations.
🎓 Qualifications
- Bachelor’s degree in Biomedical Engineering.
- Master’s or PhD preferred.
- Research experience preferred.
- Strong communication and organizational skills.
🧬 4. Project Coordinator – Core Laboratory (Navi Mumbai)
| Details | Information |
|---|---|
| Department | Imaging Services |
| Location | Navi Mumbai |
| Job ID | 11928 |
| Qualification | Biomedical Engineering |
| Experience | Research Background Preferred |
📌 Responsibilities
- Coordinate imaging-related clinical trial activities.
- Prepare project-specific reports and timelines.
- Maintain inventory and communication with sites.
- Assist internal project management activities.
🎓 Qualifications
- Bachelor’s degree in Biomedical Engineering.
- Research background preferred.
- Excellent organizational and technical skills.
🏢 Why Join Medpace?
Medpace is a globally recognized Clinical Research Organization (CRO) headquartered in Cincinnati, Ohio, operating in more than 40 countries with over 6,000 employees.
🎁 Employee Benefits
- Flexible work environment.
- Competitive salary and benefits.
- Paid time off (PTO).
- Structured career growth opportunities.
- Wellness initiatives.
- Employee appreciation programs.
🏆 Awards & Recognition
- Forbes America’s Most Successful Midsize Companies (2021–2024)
- Multiple CRO Leadership Awards from Life Science Leader magazine
📄 Resume & Interview Preparation Tips
- Add keywords like Pharmacovigilance, Argus Safety Database, Clinical Research, Drug Safety, Imaging Services, and Clinical Operations in your resume.
- Keep your resume ATS-friendly with a clean format.
- Highlight internships, clinical research projects, or pharmacovigilance exposure if available.
- Prepare for interview questions related to adverse event processing, safety databases, and project coordination.
- Practice communication and problem-solving scenarios before interviews.
📝 How to Apply
- Select your preferred Medpace role from the dropdown below.
- Read the complete job description carefully before applying.
- Prepare an updated ATS-friendly resume.
- Complete the 15-second countdown timer to unlock the application button.
- Apply only if your qualifications and skills match the role requirements.
🚀 Select Role & Apply
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Kindly read the entire job description carefully before applying. Make sure your qualifications and experience align with the role requirements. Applying thoughtfully increases your chances of being shortlisted and creates a strong professional impression.
