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Randomization & Study Product Coordinator

Medpace
Medpace
0-2 years
Not Disclosed
Bengaluru, India
10 March 2, 2026
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Randomization & Study Product Coordinator (RSPM) – Entry Level

Location: Navi Mumbai, India
Department: Data Management
Job ID: 12589
Employment Type: Full-Time, Office-Based

About the Role

ThePharmaDaily.com is inviting applications for the position of Randomization & Study Product Coordinator (RSPM) based in Navi Mumbai, India. This is an entry-level opportunity ideal for life sciences graduates seeking to build a long-term career in clinical research, clinical trial randomization systems, and investigational product management.

In this role, you will work closely with cross-functional project teams to ensure the accuracy of randomization and study product management (RSPM) system data, while supporting investigational product logistics across global clinical trials. This position offers structured onboarding and comprehensive training, enabling new hires to develop expertise in interactive response technology (IRT), clinical supply management, and trial operations.

Key Responsibilities

  • Provide operational support for Randomization & Study Product Management (RSPM) activities

  • Assist in clinical study product management and tracking

  • Support Project Managers in system design, configuration, and study set-up

  • Collaborate with sponsors and internal stakeholders to gather requirements and respond to inquiries

  • Prepare and maintain study-specific documentation

  • Ensure accurate maintenance of trial documentation and system records

  • Contribute to assigned clinical data and system-related projects

Eligibility & Qualifications

  • Bachelor’s degree in Life Sciences, Pharmacy, Biotechnology, Clinical Research, or a related field (mandatory)

  • Basic understanding of clinical research methodologies and clinical trial processes

  • Advanced working knowledge of Microsoft Excel

  • Strong analytical mindset with exceptional attention to detail

  • Effective communication and documentation skills

Experience Required

  • 0–2 years of experience in clinical research, data management, or related domains

  • Fresh graduates with strong academic backgrounds are encouraged to apply

About Medpace

Medpace is a global full-service Clinical Contract Research Organization (CRO) providing Phase I–IV clinical development services to biotechnology, pharmaceutical, and medical device companies. With headquarters in Cincinnati, Ohio, and operations across 40+ countries, Medpace employs over 5,000 professionals worldwide.

The organization supports multiple therapeutic areas including oncology, cardiology, metabolic diseases, endocrinology, CNS disorders, anti-viral, and anti-infective research. Through scientific rigor and operational excellence, Medpace accelerates the development of safe and effective medical therapies globally.

Why Join This Opportunity?

  • Structured career progression in clinical trial operations

  • Comprehensive onboarding and domain-specific training

  • Competitive compensation and benefits

  • Flexible work environment

  • Performance-driven growth opportunities

  • Employee wellness initiatives and recognition programs

Industry Recognition

The organization has been consistently recognized by Forbes as one of America’s Most Successful Midsize Companies (2021–2024) and has received multiple CRO Leadership Awards for expertise, quality, reliability, and operational excellence.

Application Process

Applications will be reviewed by the recruitment team. Shortlisted candidates will be contacted for further assessment and interview processes.

This role is ideal for candidates seeking to enter the pharmaceutical and clinical research industry in India, with a focus on randomization systems, clinical supply management, and global clinical trial support.