Randomization & Study Product Coordinator
Medpace is hiring a Randomization & Study Product (RSP) Coordinator in Navi Mumbai. This entry-level Clinical Research opportunity is ideal for Life Sciences and Pharmacy graduates looking to build a career in Clinical Trial Operations, IRT/RTSM Systems, Randomization Management, Study Product Management, and Data Management.
As a global CRO, Medpace provides structured training, global project exposure, and long-term career growth opportunities across Phase I–IV clinical trials.
📋 Job Overview
| Particulars | Details |
|---|---|
| Company | Medpace |
| Position | Randomization & Study Product Coordinator |
| Location | Navi Mumbai |
| Department | Data Management |
| Experience | 0–1 Years |
| Employment Type | Full-Time |
| Work Mode | Office Based |
| Application Mode | Online Application |
💼 Key Responsibilities
- Support Randomization & Study Product Management Activities.
- Assist in Clinical Trial Randomization System Setup.
- Support IRT/RTSM System Configuration and Validation.
- Coordinate with Project Managers and Study Teams.
- Gather and Document Study Requirements.
- Create and Maintain Study Documentation.
- Ensure Accurate Data Entry and System Compliance.
- Track Study Product Allocation Activities.
- Support Global Clinical Trial Projects.
- Maintain Regulatory-Compliant Documentation.
🎓 Eligibility Criteria
Educational Qualification
- B.Pharm
- M.Pharm
- Pharm.D
- B.Sc Life Sciences
- M.Sc Life Sciences
- Biotechnology Graduates
Experience
- Freshers Can Apply
- 0–1 Year Experience Preferred
- Clinical Research Knowledge Preferred
🧠 Required Skills
- Clinical Research Fundamentals
- Microsoft Excel
- Data Management
- Documentation Skills
- Analytical Thinking
- Attention to Detail
- Communication Skills
- Project Coordination
- Clinical Trial Processes
- Problem Solving Skills
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💰 Salary & Benefits
Based on industry benchmarks for entry-level Clinical Research and Data Management roles:
Estimated Salary: ₹3.5 LPA – ₹5.5 LPA
Actual compensation may vary depending on qualifications, skills, and company policies.
Employee Benefits
- Structured Training Program
- Global Clinical Trial Exposure
- Career Growth Opportunities
- Paid Time Off (PTO)
- Employee Wellness Programs
- Recognition & Reward Programs
- Learning & Development Support
- Work with International Study Teams
🌟 Why Join Medpace?
- Work with a Leading Global CRO.
- Gain Exposure to Phase I–IV Clinical Trials.
- Learn IRT/RTSM and Clinical Supply Processes.
- Excellent Entry Point into Clinical Research.
- Strong Internal Training and Mentorship.
- Exposure to Oncology, CNS, Cardiology, and Rare Disease Studies.
- Global Career Development Opportunities.
- Collaborative and Growth-Oriented Environment.
📈 Career Growth Opportunities
This role can lead to:
- Clinical Trial Associate (CTA)
- Clinical Data Coordinator
- Clinical Data Manager
- IRT/RTSM Specialist
- Clinical Project Coordinator
- Study Start-Up Associate
- Clinical Operations Associate
- Clinical Project Manager
📑 Resume Tips for Clinical Research Freshers
- Highlight Clinical Research Knowledge.
- Mention GCP Certification if Available.
- Include Academic Projects and Internships.
- Showcase Advanced Excel Skills.
- Mention Documentation and Data Handling Experience.
- Keep Resume ATS-Friendly and Achievement Focused.
Before applying, read:
Healthcare & Pharma Job Application Guide🎯 Interview Tips for RSP Coordinator
Candidates preparing for the Medpace interview should focus on:
- Clinical Trial Phases (I–IV).
- Basic ICH-GCP Guidelines.
- Randomization Concepts in Clinical Trials.
- IRT and RTSM Basics.
- Study Drug Accountability.
- Clinical Trial Documentation.
- Excel Functions and Reporting.
- Data Integrity Principles.
- Problem-Solving Scenarios.
- HR and Behavioral Questions.
Practice using:
Clinical Research Career Guide📌 How to Apply?
Interested candidates should prepare an updated resume highlighting clinical research knowledge, documentation skills, analytical abilities, and Excel proficiency.
Before applying, read:
Healthcare & Pharma Job Application Guide🚀 Apply Now
Interested and eligible candidates can apply through the official Medpace Careers portal.
Apply for Randomization & Study Product Coordinator📚 Related Resources from HiTechPlus
❓ Frequently Asked Questions
Q. Can freshers apply?
Yes. Freshers and candidates with up to 1 year of experience are eligible.
Q. Which qualifications are eligible?
B.Pharm, M.Pharm, Pharm.D, B.Sc, M.Sc Life Sciences, and Biotechnology graduates.
Q. What is the expected salary?
Approximately ₹3.5–5.5 LPA depending on qualifications and company policies.
Q. What is IRT/RTSM?
IRT (Interactive Response Technology) and RTSM (Randomization & Trial Supply Management) systems are used to manage patient randomization and study drug allocation in clinical trials.
Q. Is this a good entry-level clinical research role?
Yes. It offers strong exposure to Clinical Operations, Clinical Data Management, Randomization Systems, and Global Clinical Trials.
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