Clinical Trial Management Job at Medpace in Navi Mumbai | Apply Now to unleash your CRO Careers!
Medpace is seeking a full-time Associate Clinical Trial Manager (aCTM) in Navi Mumbai, India, for candidates with PhD or Post-Doctoral experience in Cardiovascular, Renal, Metabolic, or Gastrointestinal research. This role offers a unique opportunity for recent graduates to gain hands-on experience in clinical trial management, collaborate with global teams, and advance their CRO careers in the biotech and pharmaceutical industry.
Job Description:
- Job Title: Associate Clinical Trial Manager – PhD / Post-Doc (Cardiovascular/Renal/Metabolic/Gastrointestinal)
- Location: Navi Mumbai, India
- Job Category: Clinical Trial Management
- Job ID: 10936
- Employment Type: Full-time
- Industry: Biotech / Pharmaceutical CRO
Clinical Trial Management Job Summary:
Medpace is currently seeking candidates with PhDs and/or Post-Doctoral research experience in Cardiovascular/Renal/Metabolic/Gastrointestinal areas to join our Clinical Trial Management team in Navi Mumbai. The Associate Clinical Trial Manager will be responsible for supporting project coordinators and clinical trial managers in various project management activities. This role offers an excellent opportunity for recent PhD graduates to kickstart their career in a dynamic industry and work on cutting-edge therapeutic research.
About the Company:
Medpace is a full-service clinical contract research organization (CRO) located in Navi Mumbai, India. We provide Phase I-IV clinical development services to biotechnology, pharmaceutical, and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through a scientific and disciplined approach. With expertise across major areas including oncology, cardiology, metabolic disease, and more, we are dedicated to making a positive impact on patients’ lives worldwide.
Educational Requirements for the Clinical Trial Management Job:
- PhD in Life Sciences
- Post-Doctoral research experience in Cardiovascular, Renal, Metabolic, or Gastrointestinal areas
Key Responsibilities for the Clinical Trial Management Job:
- Communicate and collaborate on global study activities with Project Coordinators and Clinical Trial Managers
- Ensure timely and accurate completion of recurring tasks
- Compile and maintain project-specific status reports within the clinical trial management system
- Interact with internal teams, sponsors, study sites, and third-party vendors
- Provide oversight and quality control of internal regulatory filing systems
- Manage study supplies and maintain project timelines
- Coordinate project meetings and produce high-quality minutes
Skills Required for the Clinical Trial Management Job:
- Fluent in English with strong presentation skills
- Ability to work in a fast-paced, dynamic international environment
- Proficiency in computer applications (Word, Excel, databases, Windows)
- Strong organizational and communication skills
- Prior CRO or pharmaceutical industry experience is a plus
How to Apply for the Clinical Trial Management Job?
Interested candidates can apply online via Medpace’s official careers portal. Ensure your CV highlights PhD/Post-Doctoral research experience in relevant therapeutic areas.
Why Medpace?
Medpace offers a flexible work environment, competitive compensation and benefits packages, structured career paths for professional growth, employee appreciation events, and health and wellness initiatives. Join us and make a difference in the lives of patients around the world.
Perks of Medpace:
- Flexible work environment
- Competitive compensation and benefits
- Structured career growth
- Employee appreciation events
- Health and wellness initiatives
