Clinical Research Job at Medpace
A rare chance has emerged for experienced Clinical Trial Managers to join Medpace in Navi Mumbai, India. This leading CRO is seeking professionals with expertise in Cardiovascular, Renal, Metabolic, or Gastrointestinal areas to contribute to their Clinical Research Job Management Group. Interested candidates are encouraged to apply soon.
About Medpace:
Medpace is a full-service clinical contract research organisation (CRO) providing phase I-IV clinical development services to the biotechnology, pharmaceutical, and medical device industries. The organisation is dedicated to accelerating the global development of safe and effective medical therapeutics through the advancement of clinical research. With a presence in over 40 countries and a workforce of more than 6,500 employees, Medpace leverages in-country regulatory and therapeutic expertise across major therapeutic areas, including oncology, cardiology, and infectious diseases. The headquarters is located in Cincinnati, Ohio.
Job Details:
- Location: Navi Mumbai, India
- Categories: Clinical Trial Management
- Req ID: 11922
Job Description:
Medpace is continuing to add Clinical Trial Managers of different experience levels to join their Clinical Trial Management Group in the Navi Mumbai, India Office. Clinical Trial Managers with expertise in Cardiovascular, Renal, Metabolic, or Gastrointestinal-related studies are welcome to continue to work in their area of expertise or to expand to a new therapeutic area.
Key Responsibilities:
- Manage and provide accountability for 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, 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 management of study vendor and managing site quality, including direct supervision of project Clinical Research Associates and monitoring deliverables.
Eligibility Criteria for this Clinical Research Job:
- Bachelor’s degree in a health or life science-related field; Advanced degree in a health or life science-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 good written and spoken English.
- Flexible, accountable, and comfortable working in a global environment.
Skills Required for this Clinical Research Job:
- Strong leadership and team management skills.
- Excellent organisational and multitasking abilities.
- Proficiency in clinical trial management software and tools.
- Strong problem-solving and decision-making skills.
- Ability to work effectively in a fast-paced and dynamic environment.
- Strong interpersonal and communication skills.
