Medpace, a globally recognized Contract Research Organization (CRO), is expanding its India operations and hiring for 8 key positions in Navi Mumbai across Clinical Safety, Pharmacovigilance, Medical Writing, Data Management, Core Laboratory, and Programming functions.
This recruitment drive is an excellent opportunity for pharmacy, life science, nursing, biomedical, and data professionals seeking long-term career growth in the clinical research industry.
With over 30+ years of global CRO experience, Medpace offers structured career paths, competitive compensation, and exposure to international clinical trials across oncology, cardiology, CNS, infectious diseases, and more.
๐ Open Positions at Medpace (Navi Mumbai)
1๏ธโฃ Safety Database Specialist โ Clinical Safety
Experience: 1โ2 years
Key Skills: Argus, Argus J, SQL, OBIEE, UAT, Safety Reports (DSUR, PSUR, PBRER)
Responsibilities
- Configure studies, products, and licenses in Argus
- Generate safety reports and analytics
- Perform UAT and resolve database issues
- Support audits, inspections, SOPs, and training
2๏ธโฃ Drug Safety Specialist / Clinical Safety Coordinator
Preferred Background: Nursing, Pharmacy, Life Sciences
Responsibilities
- Process AE/SAE cases
- Write safety narratives
- Collaborate with clinical sites
- Support post-marketing pharmacovigilance
3๏ธโฃ Medical Writer โ Core Labs
Qualification: Masterโs in Health or Science
Responsibilities
- Develop and QC clinical documents
- Maintain audit trails
- Support data analysis planning
4๏ธโฃ Project Coordinator โ Core Laboratory (Imaging)
Qualification: Biomedical Engineering (Bachelorโs/Masterโs)
Responsibilities
- Manage imaging study timelines
- Coordinate with sites and internal teams
- Maintain imaging inventory
5๏ธโฃ Database Programmer โ Data Management
Skills: SQL, C#, Clinical Databases
Responsibilities
- Develop and validate clinical databases
- Design eCRFs and edit checks
- Provide technical support to DM teams
6๏ธโฃ Data Coordinator โ Core Laboratory
Experience: 1โ2 years preferred
Responsibilities
- Data validation and cleanup
- Prepare DM documents
- Handle external data transfers
7๏ธโฃ Data Coordinator โ Data Management
Skills: Medidata RAVE, Clinical Data Cleaning
Responsibilities
- Track EDC metrics
- Resolve data queries
- Reconcile clinical data
8๏ธโฃ SAS Programmer โ Core Laboratory
Requirement: SAS Certification
Responsibilities
- Program and validate mapped databases
- Prepare data transfer specifications
- Coordinate with Data Management teams
๐ Eligibility & Qualifications (Summary)
- Degrees: B.Pharm, M.Pharm, MSc, Nursing, Biomedical, Life Sciences, IT, Math, Statistics
- Freshers to 1โ2 years experience for most roles
- Strong knowledge of clinical research, pharmacovigilance, databases, or programming
- Excellent communication and attention to detail
๐ผ Why Join Medpace?
- Flexible work environment
- Competitive salary & benefits
- Structured career growth paths
- Global exposure to Phase IโIV trials
- Employee wellness initiatives
- Forbes-recognized CRO (2021โ2024)
๐ฐ Estimated Salary Range (India)
- โน4.5 LPA โ โน10 LPA (depending on role, skills, and experience)
๐ How to Apply
Application Link for Safety Database Specialist โ Clinical Safety
Application Link for Drug Safety Specialist / Clinical Safety Coordinator
Application Link for Medical Writer โ Core Labs
Application Link for Project Coordinator โ Core Laboratory (Imaging)
Application Link for Database Programmer โ Data Management
Application Link for Data Coordinator โ Core Laboratory
Application Link for Data Coordinator โ Data Management
Application Link for SAS Programmer โ Core Laboratory
