Medpace Hiring Randomization & Study Product Coordinator
Are you seeking Medpace Careers India or an Entry-Level Clinical Research Job in Mumbai? Leading global clinical contract research organization (CRO) Medpace is hiring a Randomization & Study Product (RSP) Coordinator for its Data Management and Randomization operations at its Navi Mumbai office.
This entry-level clinical study coordinator vacancy is ideal for fresh graduates holding a degree in Life Sciences who possess advanced knowledge of MS Excel and have high attention to detail. New hires undergo a detailed onboarding program to become experts in global trial randomization systems. To draft a resume detailing your laboratory database or administrative coordination milestones, read our guidelines on how to apply for healthcare and pharma jobs online.
📋 Job Details
| Particular | Details |
|---|---|
| Company | Medpace Clinical Research India Private Limited |
| Position | Randomization & Study Product (RSP) Coordinator |
| Job Location | Navi Mumbai, Maharashtra (Aurum Qpark, Ghansoli) |
| Employment Type | Full-Time |
| Experience Required | Entry Level (Freshers Eligible) |
| Qualifications | Bachelor's Degree in Life Sciences or a related field (mandatory) |
| Industry Type | Clinical Research / CRO Operations |
| Department | Randomization & Study Product Management (RSPM) |
💼 Key Responsibilities
- RSPM Operations: General support for Randomization and Study Product Management activities to ensure study database accuracy.
- Product Tracking: Manage and track investigational drug products and clinical devices assigned to active study protocols.
- System Setup: Assist Project Managers in initial randomization system design and clinical database configuration.
- Requirement Gathering: Work with study sponsors and clients to gather workflow requirements, responding to process queries.
- Dossier Compilation: Create and maintain study-specific documents, trial guidelines, and tracking spreadsheets.
- Documentation Maintenance: File, verify, and maintain essential trial study product documents.
To learn how clinical coordinator and data analyst salaries compare to specialized pharmacovigilance drug safety associate and medical writing structures, read our report on Pharmacovigilance Salary: India vs USA.
🎓 Required Qualifications & Skills
- Education: Bachelor's degree (mandatory) in Life Sciences (Biotech, Microbiology, Biochemistry, etc.) or related fields.
- Methodology Knowledge: Basic understanding of clinical trial phases, research methodologies, and GCP standards.
- Excel Skills: Advanced working knowledge of Microsoft Excel (VLOOKUP, Pivot Tables, formulas) for data tracking.
- Traits: High level of organization, attention to detail, and ability to handle multi-tasking under deadlines.
For science graduates exploring technology-driven clinical operations pathways compared to laboratory formulation tracks, read our analysis on B.Pharm Careers after Graduation: India vs USA.
🎁 Why Join Medpace?
- Structured onboarding and specialized training in clinical randomization databases.
- Work with a top global CRO employing over 6,000 professionals in 40+ countries.
- Develop a strong foundation in clinical supply chain, randomization, and site operations.
- Competitive compensation, comprehensive PTO, and wellness perks.
To review your basic understanding of clinical study protocols, adverse event reporting, and GCP guidelines before your interviews, try our interactive Clinical Trial Assistant (CTA) Quiz.
💡 RSP Coordinator vs Healthcare IT
RSP Coordinators design randomization systems, coordinate study drug inventories, and maintain trial databases to manage drug studies, whereas Healthcare IT professionals support software deployments. To explore these differences, read our comparison on Healthcare IT vs Clinical Healthcare.
📝 Resume Tips for Medpace RSP Candidates
- Highlight Excel Projects: Emphasize any university projects or internships where you cleaned datasets, created charts, or managed spreadsheets.
- Specify System Knowledge: Mention if you are familiar with basic database concepts, clinical trials registries, or clinical research terminology.
- Demonstrate Detail Orientation: Highlight roles or situations where checking files for accuracy and verifying inventory lists was a core duty.
💬 Medpace RSP Coordinator Interview Questions
- Q1. What is the role of Randomization in a clinical trial?
Answer Guidance: Randomization is the process of assigning trial participants to treatment or control groups by chance. This minimizes bias, ensures the comparability of groups, and validates the statistical results of the trial. - Q2. How would you handle a discrepancy between the study product shipment inventory list and the actual physical stock?
Answer Guidance: I would isolate the shipment immediately, document the discrepancy in our tracking file, check the batch/lot numbers, and escalate the event to the Project Manager and site coordinator to investigate the database log details. - Q3. Why is Microsoft Excel such a critical tool in clinical study product tracking?
Answer Guidance: Excel allows coordinators to maintain real-time logs, calculate product expiration windows, perform inventory tracking reconciliation, and generate summary tables to monitor study product usage across multiple investigational sites.
🚀 How to Apply?
Interested and eligible candidates can submit their applications directly via Medpace's official careers portal. Click the button below to apply:
Apply Online – Medpace Official Careers Portal❓ Frequently Asked Questions
Q. Do I need experience in randomization systems to apply for this Medpace coordinator role?
No. This is an entry-level position. Medpace provides a comprehensive onboarding and training program for new hires.
Q. Which degrees are eligible for the RSP Coordinator opening?
A Bachelor's degree in Life Sciences (or related science/health fields) is mandatory to apply.
Q. Where is this position based?
This is a full-time, office-based position located at Medpace's office in Navi Mumbai, Maharashtra, India.
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