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.
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
