If you are a life sciences graduate looking to enter the world of clinical research and data management, an exciting opportunity awaits you in Navi Mumbai, India. The role of Randomization & Study Product Coordinator (RSP Coordinator) at Medpace is a perfect starting point for candidates who are detail-oriented, analytical, and eager to build a long-term career in the clinical research industry 📊🧬.
This position offers hands-on exposure to clinical trial operations, study product management, and randomization systems—critical components of modern clinical development. Let’s explore why this role could be a great step forward in your professional journey.
🧪 About the Role: Randomization & Study Product Coordinator
A Randomization & Study Product Coordinator plays a key role in ensuring that clinical trial data and study product information are accurate, compliant, and well-managed throughout the lifecycle of a study.
This is an entry-level, full-time, office-based role, designed for individuals who want to grow into subject-matter experts through structured training and real-world project exposure.
You will work closely with project managers, internal teams, and external clients to support clinical studies from setup to execution. This position is ideal for fresh graduates or early-career professionals who enjoy structured work, problem-solving, and collaboration 🤝.
📍 Location Advantage: Navi Mumbai
Navi Mumbai has emerged as a major hub for pharmaceutical, biotechnology, and CRO industries. With excellent infrastructure, connectivity, and career growth opportunities, it is an ideal location for clinical research professionals.
Working in Navi Mumbai also allows exposure to global projects while being based in India 🌆.
📝 Key Responsibilities
As a Randomization & Study Product Coordinator, your day-to-day responsibilities may include:
🔹 Supporting randomization and study product management activities
🔹 Assisting with system setup and design under the guidance of project managers
🔹 Managing and maintaining study-related data within specialized systems
🔹 Coordinating with clients to gather study requirements and respond to queries
🔹 Preparing and maintaining study-specific documentation
🔹 Ensuring accuracy, consistency, and compliance in all records
🔹 Supporting additional projects assigned by the team
This role demands precision, consistency, and a proactive mindset to ensure smooth clinical trial operations ✅.
🎓 Educational Qualifications & Skills Required
To be eligible for this role, candidates should meet the following criteria:
✔ Bachelor’s degree in Life Sciences, Pharmacy, Biotechnology, or related fields
✔ Basic understanding of clinical research methodologies
✔ Strong working knowledge of Microsoft Excel (data handling, formulas, tracking)
✔ Excellent attention to detail and organizational skills
✔ Ability to learn new systems and adapt to evolving processes
No extensive prior experience is required, making this an excellent entry-level clinical research job 🎯.
🏢 About Medpace
Medpace is a globally recognized full-service Contract Research Organization (CRO) providing Phase I–IV clinical development services. The organization supports biotechnology, pharmaceutical, and medical device companies across therapeutic areas such as oncology, cardiology, CNS, endocrinology, and infectious diseases.
Headquartered in Cincinnati, Ohio, Medpace operates in over 40 countries and employs thousands of professionals worldwide 🌐. The company is known for its scientific rigor, structured processes, and commitment to improving patient outcomes globally.
🌟 Why Choose a Career with Medpace?
Joining Medpace means becoming part of an organization driven by People, Purpose, and Passion ❤️. Employees benefit from:
✨ Structured onboarding and in-depth training programs
✨ Exposure to global clinical trials
✨ Clear career progression pathways
✨ A collaborative and professional work environment
✨ Opportunity to contribute to life-changing medical research
The work done today directly impacts patients and families around the world, making this career both meaningful and future-focused 🌱.
🚀 Career Growth & Future Scope
Starting as an RSP Coordinator can open doors to advanced roles in:
📌 Clinical Data Management
📌 Randomization & Trial Supply Management (RTSM)
📌 Project Coordination
📌 Clinical Operations
With experience and continuous learning, professionals can grow into senior specialist or management roles within the CRO industry.
✅ Who Should Apply?
This role is ideal for:
- Fresh graduates in life sciences or pharmacy
- Candidates seeking entry into clinical research
- Individuals who enjoy data accuracy and documentation
- Professionals aiming for long-term growth in CROs
🔗 Apply Now
Interested candidates can apply directly through the official careers page:
👉 https://careers.medpace.com/jobs/12589?lang=en-us
🏁 Final Thoughts
The Randomization & Study Product Coordinator role in Navi Mumbai is an excellent launchpad for a rewarding career in clinical research. With structured training, global exposure, and a mission-driven organization, this opportunity is perfect for those who want to make a real difference while building strong technical and professional skills 💡.
If you are passionate about science, accuracy, and healthcare innovation, this role could be your next big step forward.
