Clinical Trials Job at Medpace in Navi Mumbai | Health Science Job
Looking for a rewarding clinical trials job in India? Medpace is hiring professionals to join its Clinical Trial Management Group in Navi Mumbai. This health science job offers the opportunity to manage global clinical trials, work across multiple therapeutic areas, and contribute to high-quality clinical research. Explore exciting jobs in Mumbai with a leading CRO today.
Job Details:
- Job Position: Clinical Trial Manager
- Location: Navi Mumbai, India
- Job ID: 11922
About the Company
Medpace is a full-service clinical contract research organization (CRO) providing Phase I–IV clinical development services to the biotechnology, pharmaceutical, and medical device industries. The organization focuses on accelerating the global development of safe and effective medical therapeutics through a scientific and disciplined approach. Medpace leverages regulatory and therapeutic expertise across oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral, and anti-infective areas. Headquartered in Cincinnati, Ohio, Medpace employs more than 5,000 professionals across 40+ countries and offers leading health science jobs and jobs in Mumbai.
Qualifications
- Bachelor’s degree in a health science-related field; an advanced degree in a health-related field preferred
- At least 2 years of clinical trial management experience in the Asia Pacific region, ideally in a CRO environment
- Experience in Cardiovascular, Renal, Metabolic, or Gastrointestinal-related studies required
- Excellent communication skills, including strong written and spoken English
- Flexible, accountable, and comfortable working in a global environment
Job Description
Medpace is the leading CRO for Biotech companies and is continuing to add Clinical Trial Managers of different experience levels to join the Clinical Trial Management Group in the Navi Mumbai, India office. This clinical trials job is suitable for professionals with experience in Cardiovascular, Renal, Metabolic, or Gastrointestinal studies who wish to continue in their therapeutic area or expand into a new one. This role represents a strong opportunity among jobs in Mumbai for clinical research professionals.
Key Responsibilities
- Manage and provide accountability for the day-to-day operations of the project, as defined by the contract and according to ICH/GCP and all other applicable laws, rules, and regulations
- Serve as primary Sponsor contact for operational project-specific issues and study deliverables
- Maintain in-depth knowledge of protocol, therapeutic area, and indication
- Provide cross-functional oversight of internal project team members and deliverables, including ensuring all necessary project-specific training is provided
- Review and provide input for study protocol, edit check specifications, data analysis plan, and final study report, when applicable
- Develop operational project plans
- Manage risk assessment and execution
- Responsible for the management of the study vendor
- Manage site quality, including direct supervision of project Clinical Research Associates and monitoring deliverables
