Medpace is hiring for two clinical research and Data Management roles in Navi Mumbai, India. The company has openings for eClinical Coordinator and Randomization & Study Product Coordinator professionals within its Data Management and eClinical teams.

These Medpace jobs in Mumbai offer an opportunity for candidates with bachelor’s degrees in health-related, life science, pharmacy, clinical research, biotechnology, and related disciplines to build careers within a global Contract Research Organization (CRO).

The Randomization & Study Product Coordinator position is specifically described by Medpace as an entry-level role, making it particularly relevant for eligible early-career candidates. The eClinical Coordinator position prefers candidates with 1–2 years of pharmaceutical or CRO experience, although the wording of the job posting indicates this experience is preferred rather than explicitly mandatory.

Both positions involve clinical study systems, study documentation, project coordination, data accuracy, client requirements, and collaboration with project managers.

Vacancy 1: eClinical Coordinator

Job ID: 12323
Department: Data Management / eClinical
Location: Navi Mumbai, India
Employment: Full-Time, Office-Based
Travel: None

The eClinical Coordinator works with the eClinical Project Manager and other study team members to help ensure the accuracy of patient-reported clinical study data.

Responsibilities

• Assist the eClinical Project Manager with clinical study system design and setup.
• Create study-specific documents.
• Track important clinical study metrics.
• Support project monitoring activities.
• Coordinate with clients to obtain study requirements.
• Respond to client inquiries related to assigned activities.
• Maintain accurate and organized project information.
• Support additional eClinical and Data Management projects as assigned.

Qualifications

Candidates should have:

• Bachelor’s degree in a health-related field.
• Strong attention to detail.
• Working knowledge of Microsoft Excel and Word.
• Knowledge of medical terminology.
• Approximately 1–2 years of pharmaceutical or CRO experience is preferred.
• Mumbai-based candidates are preferred.

Relevant educational backgrounds may include B.Pharm, Pharm.D, B.Sc Life Sciences, B.Sc Biotechnology, B.Sc Microbiology, B.Sc Biochemistry, B.Sc Clinical Research, Nursing, and other relevant health-related bachelor’s degrees, subject to Medpace’s final eligibility assessment.

Vacancy 2: Randomization & Study Product Coordinator

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

Medpace is also recruiting a Randomization & Study Product (RSP) Coordinator. The role supports randomization and study product management activities while helping maintain accurate RSPM system data.

Responsibilities

• Provide general Randomization & Study Product Management support.
• Support study product management activities.
• Assist the Project Manager with study system design and setup.
• Work with clients to collect study requirements.
• Respond to client inquiries.
• Prepare study-specific documents.
• Maintain clinical study documentation.
• Ensure accurate study and system information.
• Complete additional projects and responsibilities assigned by the team.

Qualifications

Candidates should have:

• Bachelor’s degree in life sciences or a related field.
• Basic knowledge of clinical research methodologies.
• Advanced working knowledge of Microsoft Excel.
• Strong attention to detail.

Relevant degrees may include B.Pharm, Pharm.D, B.Sc Life Sciences, B.Sc Biotechnology, B.Sc Microbiology, B.Sc Biochemistry, B.Sc Clinical Research, B.Tech Biotechnology, and other related life science bachelor’s degrees, subject to employer screening.

Skills That Can Strengthen Your Application

Applicants interested in these Medpace clinical research jobs should ideally understand fundamentals such as clinical trial phases, clinical research terminology, study documentation, data quality, Microsoft Excel, and Good Clinical Practice (GCP).

For the Randomization & Study Product Coordinator role, understanding randomization, investigational product management, blinding, clinical trial supplies, and study documentation may be particularly useful.

For the eClinical Coordinator position, knowledge of eClinical systems, patient-reported data, clinical data management, medical terminology, study metrics, and documentation can help candidates prepare for the selection process.

Why Join Medpace?

Medpace highlights several career-development and employee benefits, including:

• Structured onboarding and training.
• Defined career advancement opportunities.
• On-site mentors.
• Continuous professional development.
• Cross-functional exposure to clinical research experts.
• Competitive compensation.
• Health and wellness benefits.
• Retirement and paid-time-off benefits.
• Company-sponsored social events.
• Potential occasional work-from-home flexibility for eligible positions after training.

Benefits may vary depending on location, role, and company policy.

About Medpace

Medpace is a global, full-service Contract Research Organization (CRO) providing Phase I–IV clinical development services to biotechnology, pharmaceutical, and medical device companies.

The organization supports clinical development across therapeutic areas including oncology, cardiology, metabolic and endocrine diseases, central nervous system disorders, and anti-viral and anti-infective research.

According to the supplied job information, Medpace employs more than 6,500 people across 40+ countries.

How to Apply

Application Link For eClinical Coordinator

Application Link For Randomization and Study Product Coordinator