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Medpace Hiring For Multiple Roles in CDM, Clinical Operations

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Are you looking to advance your career in the pharmaceutical or clinical research industry? Medpace, a leading global full-service clinical contract research organization (CRO), is expanding its team in Navi Mumbai, India. We are currently hiring for 5 exciting roles in Data Management, Clinical Operations, and Biometrics. If you are passionate about contributing to the development of safe and effective medical therapeutics, this is your chance to join a dynamic and growing organization.

Read on to learn more about the job openings, responsibilities, qualifications, and how to apply.

1. eClinical Coordinator

Job ID: 10890
Location: Navi Mumbai, India
Department: Data Management

Job Summary:
Join our Data Management/eClinical team as an eClinical Coordinator. This role ensures the accuracy of patient-reported data for clinical studies. If you are detail-oriented and thrive in a structured work environment, this opportunity is for you.

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Responsibilities:

  • Assist in system design and setup
  • Create study-specific documents
  • Track and provide key study metrics
  • Collaborate with clients to gather requirements and respond to inquiries

Qualifications:

  • Bachelor’s degree in a health-related field
  • Strong attention to detail and proficiency in Excel and Word
  • Knowledge of medical terminology
  • 1-2 years of experience in a pharmaceutical or CRO setting (preferred)

2. Data Review Associate

Job ID: 10929
Location: Navi Mumbai, India
Department: Data Management

Job Summary:
Work with our Global Clinical Coding & Support team to review clinical data and develop guidelines for therapeutic areas like Oncology, Hematology, and Infectious Disease.

Responsibilities:

  • Conduct comprehensive manual reviews of clinical data
  • Develop clinical review guidelines
  • Interface with the Data Management team for query resolution

Qualifications:

  • Bachelor’s degree in Nursing/Medicine or advanced clinical degree
  • Professional nursing experience, preferably in Oncology/Hematology
  • Knowledge of clinical trial processes
  • Experience with MedDRA and WHO Drug dictionaries (preferred)

3. Study Start-up Submissions Coordinator

Job ID: 11032
Location: Navi Mumbai, India
Department: Site Activation & Maintenance

Job Summary:
Play a vital role in activating investigative sites for clinical trials by preparing and submitting regulatory documentation.

Responsibilities:

  • Prepare, review, and submit regulatory documents
  • Communicate with global study teams
  • Ensure compliance with ICH-GCP and regulatory guidelines

Qualifications:

  • Bachelor’s degree in a science field
  • 1+ year of experience in a CRO, pharmaceutical company, or investigative site
  • Excellent organizational and communication skills
  • Knowledge of Microsoft Office and regulatory guidelines

4. Data Coordinator

Job ID: 10753
Location: Navi Mumbai, India
Department: Data Management

Job Summary:
Join our Data Management team to clean and reconcile clinical data while supporting departmental activities.

Responsibilities:

  • Track and maintain data metrics
  • Clean clinical databases and resolve data clarifications
  • Reconcile clinical data

Qualifications:

  • Bachelor’s degree in life sciences, pharmacy, or a health-related field
  • Knowledge of medical terminology and clinical research
  • Experience with clinical databases like Medidata RAVE (preferred)

5. Clinical Database Programmer

Job ID: 11110
Location: Navi Mumbai, India
Department: Data Management

Job Summary:
Develop and maintain clinical trial databases while providing technical support to the Data Management team.

Responsibilities:

  • Program, validate, and maintain clinical trial databases
  • Contribute to the company’s library of standard CRFs
  • Provide technical support for assigned studies

Qualifications:

  • Bachelor’s or advanced degree in Life Sciences or Computer Science
  • 1-3 years of Medidata Rave study build experience
  • Custom function (C# Programming) experience (preferred)
  • Certified Medidata Rave Study Builders (preferred)

Application Link For eClinical Coordinator

Application Link For Data Review Associate

Application Link For Study Start-up Submissions Coordinator

Application Link For Data Coordinator

Application Link For Clinical Database Programmer