Clinical Trial Manager

Responsibilities

• Act as project lead for multiservice clinical trials, including global studies
• Manage timelines, project deliverables, and interactions with sponsors
• Coordinate all contracted services for the study
• Lead a team of CRAs and manage project coordinators
• Direct operations of designated functional areas or groups
• Ensure compliance with SOPs, GCP, and GLP guidelines
• Evaluate departmental capacity and delegate workload efficiently
• Participate in Business Development, including proposal reviews and BID defense meetings

Requirements

• Bachelor’s degree in a health-related field
• Minimum 3 years of clinical trial management experience in the Asia Pacific region
• Experience in a CRO environment preferred
• Advanced knowledge of federal regulations regarding clinical studies
• Advanced knowledge of GCP and/or GLP guidelines
• Demonstrated strategic thinking and execution abilities

Preferred Qualifications

• Master’s degree or PhD

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.