Looking to start your career in clinical research and data management? Medpace is hiring a Randomization & Study Product (RSP) Coordinator in Navi Mumbai, India. This is an entry-level clinical research job ideal for life science graduates seeking opportunities in clinical trial randomization, study product management, and CRO operations.
As a global full-service CRO, Medpace offers structured training, defined career pathways, and exposure to Phase I–IV clinical trials across therapeutic areas such as oncology, cardiology, CNS, metabolic diseases, and infectious diseases.
Medpace is a global clinical contract research organization (CRO) headquartered in Cincinnati, Ohio, operating in over 40 countries with 5,000+ employees. The company supports biotechnology, pharmaceutical, and medical device industries with end-to-end clinical development services.
Recognitions include:
- Forbes’ America’s Most Successful Midsize Companies (2021–2024)
- CRO Leadership Awards by Life Science Leader
Job Overview
Position: Randomization & Study Product (RSP) Coordinator
Location: Navi Mumbai, India
Department: Data Management
Experience Level: Entry-Level
Employment Type: Full-Time (Office-Based)
This Randomization & Study Product Coordinator job in Navi Mumbai focuses on ensuring accurate system data, supporting clinical trial randomization processes, and assisting in study product management activities.
New hires undergo extensive onboarding and training, making it an excellent opportunity for fresh graduates aiming to build expertise in IRT/RTSM systems, clinical supply management, and CRO operations.
Key Responsibilities
- Provide general Randomization & Study Product Management (RSPM) support
- Assist in clinical trial randomization system setup and validation
- Support study product management activities
- Collaborate with Project Managers for system design and configuration
- Communicate with clients to gather study requirements
- Create and maintain study-specific documentation
- Ensure accurate data entry and system compliance
- Support assigned RSPM projects
This role strengthens skills in clinical data management, IRT systems, Excel-based tracking, and documentation control.
Qualifications
- Bachelor’s degree in Life Sciences or related field (B.Pharm, M.Pharm, BSc, MSc, Biotech, etc.)
- Basic understanding of clinical research methodologies
- Advanced working knowledge of Microsoft Excel
- Strong attention to detail and documentation accuracy
Candidates targeting careers in clinical trial coordination, data management, or CRO project support will find this role highly relevant.
Salary & Benefits
Estimated Salary Range (India): ₹3,50,000 – ₹5,50,000 per annum (based on industry benchmarks for entry-level CRO roles)
Medpace Perks:
- Flexible work environment
- Competitive compensation & benefits
- Structured career growth path
- Paid time off (PTO)
- Employee wellness initiatives
- Recognition and appreciation programs
Why This Role Is Important
The Randomization & Study Product Coordinator plays a critical role in:
- Ensuring proper patient randomization in clinical trials
- Maintaining compliance in study product allocation
- Supporting regulatory-ready documentation
- Enhancing data integrity across clinical development phases
This is a high-impact entry-level role within clinical data management that directly supports global drug development programs.
How to Apply
