Medpace, one of the world’s leading Contract Research Organizations (CROs), has announced exciting career opportunities for professionals in Clinical Trial Management at its Navi Mumbai office. The company is currently hiring for two positions: Associate Clinical Trial Manager (PhD/Post-Doc) and Clinical Trial Manager.
These opportunities are ideal for candidates looking to build or advance their careers in clinical research, project management, and global clinical trials. Whether you are a recent PhD graduate aiming to enter the pharmaceutical industry or an experienced Clinical Trial Manager with CRO experience, Medpace offers structured career growth, global exposure, and competitive benefits.
Job Details
| Particular | Details |
|---|---|
| Company | Medpace |
| Roles | Associate Clinical Trial Manager (PhD/Post-Doc), Clinical Trial Manager |
| Location | Navi Mumbai, Maharashtra |
| Department | Clinical Trial Management |
| Job Type | Full-Time |
| Industry | CRO / Clinical Research |
| Experience | Fresh PhD / Experienced CTMs |
| Qualification | PhD / Bachelor’s / Advanced Degree (Role-specific) |
Role 1: Associate Clinical Trial Manager (PhD/Post-Doc)
This role is designed specifically for recent PhD graduates or Post-Doctoral researchers interested in transitioning from academia into the pharmaceutical and clinical research industry.
Key Responsibilities
- Support Clinical Trial Managers in global clinical studies.
- Coordinate with sponsors, project teams, study sites and vendors.
- Prepare and maintain project status reports.
- Manage study timelines and documentation.
- Oversee regulatory filing systems.
- Coordinate project meetings and prepare meeting minutes.
- Manage study supplies and operational activities.
- Ensure high-quality project administration.
Eligibility Criteria
Candidates should have:
- PhD in Life Sciences.
- Research experience in Cardiovascular, Renal, Metabolic or Gastrointestinal therapeutic areas.
- Strong communication and presentation skills.
- Excellent knowledge of MS Office, Excel and databases.
- Good organizational and analytical skills.
- Prior CRO experience is not mandatory.
Role 2: Clinical Trial Manager
Medpace is also recruiting experienced Clinical Trial Managers to lead international clinical studies across Asia-Pacific.
Key Responsibilities
- Manage end-to-end clinical trial operations.
- Act as the primary sponsor contact.
- Ensure ICH-GCP compliance.
- Develop operational project plans.
- Lead cross-functional project teams.
- Manage vendors and clinical research associates.
- Perform project risk management.
- Maintain study quality and timelines.
Eligibility Criteria
Applicants should possess:
- Bachelor’s degree in Health Sciences or Life Sciences.
- Advanced degree preferred.
- Minimum 2 years of Clinical Trial Management experience.
- Experience in CRO preferred.
- Therapeutic expertise in Cardiovascular, Renal, Metabolic or Gastrointestinal studies.
- Excellent English communication skills.
Why Join Medpace?
Medpace offers excellent career development opportunities in a truly global environment.
Employee Benefits
- Flexible work environment
- Competitive salary package
- Performance-based benefits
- Paid Time Off (PTO)
- Structured career progression
- International project exposure
- Employee wellness initiatives
- Learning and development programs
- Employee appreciation events
About Medpace
Medpace is a globally recognized Contract Research Organization (CRO) headquartered in Cincinnati, Ohio. The company provides Phase IโIV clinical development services for biotechnology, pharmaceutical, and medical device companies across more than 40 countries with over 6,000 employees worldwide.
Medpace has consistently been recognized by Forbes as one of America’s Most Successful Midsize Companies and has received multiple CRO Leadership Awards for excellence in quality, expertise, and reliability.
How to Apply
Application Link For Associate Clinical Trial Manager (PhD/Post-Doc)
Application Link For Clinical Trial Manager