Clinical Research Job at Medpace
Looking for a rewarding Clinical Research Job with a globally recognized CRO? Here’s an excellent opportunity for professionals seeking advancement in Life Science Careers. Medpace Careers has announced openings for Clinical Trial Managers in Navi Mumbai, offering candidates the chance to work on international clinical studies across cardiovascular, renal, metabolic, and gastrointestinal therapeutic areas. If you have experience in clinical trial management and want to contribute to global healthcare innovation, this Clinical Research Job could be the perfect next step in your professional journey.
About Medpace Careers
Medpace is a full-service Clinical Research Organization (CRO) providing Phase I-IV clinical development services to biotechnology, pharmaceutical, and medical device companies worldwide. Headquartered in Cincinnati, Ohio, the company employs over 6,000 professionals across more than 40 countries.
Through Medpace Careers, professionals gain access to cutting-edge research projects that accelerate the development of safe and effective therapies. The organization is recognized globally for excellence in clinical research, quality delivery, and scientific expertise.
Job Details:
- Job Title: Clinical Trial Manager
- Location: Navi Mumbai, India
- Department: Clinical Trial Management
- Job ID: 11922
Job Summary
Medpace, a leading Contract Research Organization (CRO) for biotechnology companies, continues to expand its Clinical Trial Management Group and is seeking Clinical Trial Managers of varying experience levels to join its Navi Mumbai, India office.
Professionals with expertise in Cardiovascular, Renal, Metabolic, or Gastrointestinal therapeutic areas are encouraged to continue working within their specialties or broaden their experience by expanding into new therapeutic areas.
Responsibilities
The Clinical Trial Manager will:
- Manage and maintain accountability for the day-to-day operations of assigned projects, as defined by the contract and in accordance with ICH/GCP and all applicable laws, rules, and regulations.
- Serve as the primary Sponsor contact for operational project-specific issues and study deliverables.
- Maintain in-depth knowledge of study protocols, therapeutic areas, and indications.
- Provide cross-functional oversight of internal project team members and deliverables, ensuring all necessary project-specific training is delivered.
- Review and provide input on study protocols, edit check specifications, data analysis plans, and final study reports, where applicable.
- Develop operational project plans.
- Manage risk assessment and execution activities.
- Oversee study vendor management.
- Manage site quality, including direct supervision of project Clinical Research Associates and monitoring deliverables.
Qualifications
Candidates should possess:
- A Bachelor’s degree in a health or life science-related field; an advanced degree in a health or life science-related field is preferred.
- At least 2 years of clinical trial management experience within the Asia Pacific region, ideally in a CRO environment.
- Experience in Cardiovascular, Renal, Metabolic, or Gastrointestinal-related studies.
- Excellent communication skills, including strong written and spoken English.
- Flexibility, accountability, and the ability to work effectively in a global environment.
Why Medpace?
People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today.
Over the past 30+ years, Medpace has positively impacted the lives of countless patients and families facing hundreds of diseases across key therapeutic areas. The work being conducted today is focused on improving the lives of people living with illness and disease in the future.
Medpace Perks
- Flexible work environment
- Competitive compensation and benefits package
- Competitive PTO packages
- Structured career paths with opportunities for professional growth
- Company-sponsored employee appreciation events
- Employee health and wellness initiatives
