Medpace Hiring Randomization & Study Product Coordinator | Life Sciences Freshers
- Medpace Hiring Randomization & Study Product Coordinator | Life Sciences Freshers | Navi Mumbai
- Company Overview
- Job Role & Responsibilities
- Core Responsibilities
- Eligibility & Qualifications
- Educational Qualification
- Experience
- Required Skills
- Location & Employment Details
- Application Process
- Career Growth Opportunities
- Frequently Asked Questions (FAQs)
- 1. Is this role suitable for freshers?
- 2. Is prior clinical trial experience mandatory?
- 3. Is this a remote role?
- 4. What technical skills are important?
- 5. Does Medpace provide training?
- Summary Table
Medpace Hiring Randomization & Study Product Coordinator | Life Sciences Freshers | Navi Mumbai
Medpace is hiring for the position of Randomization & Study Product (RSP) Coordinator in the Data Management department at Navi Mumbai, India. This is a full-time, office-based entry-level opportunity designed for life sciences graduates who want to build a career in clinical research, clinical trial operations, and study product management.
Freshers with a Bachelor’s degree in Life Sciences or related fields are eligible to apply. This role offers structured onboarding and intensive training to develop expertise in randomization systems, investigational product management, and clinical trial data coordination within a global CRO environment.
Company Overview
entity[“organization”,”Medpace”,”clinical research organization”] is a full-service clinical contract research organization (CRO) providing Phase I–IV clinical development services to pharmaceutical, biotechnology, and medical device companies worldwide. Headquartered in Cincinnati, Ohio, Medpace employs more than 5,000 professionals across 40+ countries.
The organization specializes in accelerating the global development of safe and effective medical therapeutics through a disciplined scientific approach. Therapeutic expertise spans oncology, cardiology, metabolic disorders, endocrinology, CNS, anti-viral, and anti-infective research.
Recognized by Forbes as one of America’s Most Successful Midsize Companies and consistently awarded CRO Leadership honors, Medpace has built a strong reputation for quality, regulatory excellence, and clinical research innovation.
Job Role & Responsibilities
The Randomization & Study Product Coordinator supports clinical trial randomization systems and investigational product supply management activities. The role ensures system data accuracy, proper study documentation, and coordination with project teams and sponsors.
Core Responsibilities
- Provide general support for randomization and study product management activities.
- Assist in study product supply tracking and accountability.
- Support Project Managers in system design and set-up activities.
- Work closely with clients to gather requirements and respond to study-related inquiries.
- Create and maintain study-specific documentation.
- Ensure accuracy and integrity of RSPM system data.
- Maintain organized study documentation and regulatory-compliant records.
- Contribute to additional assigned projects within clinical trial operations.
This position plays a critical role in ensuring that clinical trial participants are properly randomized and that investigational products are managed accurately throughout the trial lifecycle.
Eligibility & Qualifications
Educational Qualification
Bachelor’s degree (required) in Life Sciences or related fields such as:
B.Pharm, M.Pharm, BSc Biotechnology, BSc Microbiology, BSc Biochemistry, BSc Life Sciences, MSc Biotechnology, MSc Microbiology, MSc Biochemistry, PharmD, Clinical Research, Biomedical Sciences.
Experience
- Entry-level role.
- Freshers are eligible.
- Basic knowledge of clinical research methodologies preferred.
Required Skills
- Advanced working knowledge of Microsoft Excel.
- Strong analytical and documentation skills.
- Attention to detail and structured thinking.
- Ability to work in a dynamic, process-driven environment.
- Strong communication and coordination skills.
Candidates with exposure to clinical trials, randomization systems, or investigational product handling during internships will have an added advantage.
Location & Employment Details
- Location: Navi Mumbai, India
- Department: Data Management
- Employment Type: Full-Time
- Work Mode: Office-Based
- Job ID: 12589
Application Process
Interested candidates can apply directly through the official Medpace careers portal using the link below:
Apply Here: https://careers.medpace.com/jobs/12589?lang=en-us
Shortlisted candidates will be contacted by the Medpace recruitment team for further steps in the hiring process.
Career Growth Opportunities
With experience, professionals can progress into roles such as:
- Clinical Trial Coordinator
- Clinical Data Management Specialist
- Randomization & Trial Supply Manager
- Clinical Project Associate
- Regulatory Operations Associate
The clinical research industry continues to expand globally, offering long-term career stability and advancement in drug development and medical device trials.
Frequently Asked Questions (FAQs)
1. Is this role suitable for freshers?
Yes, this is an entry-level position and fresh graduates are eligible to apply.
2. Is prior clinical trial experience mandatory?
No, but basic knowledge of clinical research methodologies is preferred.
3. Is this a remote role?
No, this is an office-based position in Navi Mumbai.
4. What technical skills are important?
Advanced Excel skills and strong documentation capabilities are important.
5. Does Medpace provide training?
Yes, new hires undergo structured onboarding and training to develop expertise in randomization and study product systems.
Summary Table
| Company | Medpace |
| Vacancies | Randomization & Study Product Coordinator |
| Required Education | B.Pharm, M.Pharm, BSc/MSc Biotechnology, Microbiology, Biochemistry, Life Sciences, PharmD, Clinical Research |
| Experience | Entry-level; Freshers eligible; Basic clinical research knowledge preferred |
To apply for this job please visit careers.medpace.com.
