Clinical Trial Manager

About This Role

Being a Clinical Trial Manager involves leading the daily operations of clinical trials for biotechnology companies, ensuring compliance with regulations and serving as the main contact for sponsors. This role suits experienced professionals in clinical trial management, particularly those with expertise in cardiovascular, renal, metabolic, or gastrointestinal studies.

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, which includes 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
• Manage site quality, including direct supervision of project Clinical Research Associates and monitoring deliverables

Requirements

• Bachelor's degree in a health or life science-related field
• 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
• Excellent communication skills including good written and spoken English
• Flexible, accountable and comfortable in working in a global environment

Nice to have:

• Advanced degree in a health or life science-related field

Benefits

• Competitive compensation programs that recognize and reward performance
• Comprehensive health, wellness, retirement, and PTO benefits
• Office-based culture with occasional work-from-home that provides flexibility for eligible positions after training
• Company-sponsored social events

Application Process

• A Medpace team member will review your application and if your profile matches current needs, you will be contacted for an interview

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. Its mission is to accelerate the global development of safe and effective medical therapeutics through the advancement of clinical research. Headquartered in Cincinnati, Ohio, it employs more than 6,500 people across 40+ countries.