Associate Clinical Trial Manager

Responsibilities

• Communicate and collaborate on global study activities, working closely with Project Coordinators and Clinical Trial Managers
• Ensure timely delivery of recurrent tasks with a high degree of accuracy
• Compile and maintain project-specific status reports within the clinical trial management system
• Interact with internal project teams, Sponsors, study sites, and third-party vendors
• Provide oversight and quality control of the internal regulatory filing system
• Manage study supplies and create/maintain project timelines
• Coordinate project meetings and produce high-quality minutes

Requirements

• PhD in Life Sciences
• Research experience in Cardiovascular, Renal, Metabolic, or Gastrointestinal areas
• Fluency in English with strong presentation skills
• Proficiency in Microsoft Excel, Windows, and general word-processing/database tools
• Ability to work in a fast-paced, dynamic international environment

Preferred Qualifications

• Prior experience within the CRO or pharmaceutical industry

Benefits

• Competitive compensation and benefits package
• Competitive PTO packages
• Structured career paths with opportunities for professional growth
• Flexible work environment
• Company-sponsored employee appreciation events and wellness initiatives

About the Company

Medpace is a leading full-service clinical contract research organization (CRO) providing Phase I-IV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Headquartered in Cincinnati, Ohio, with over 6,000 employees across 40+ countries, Medpace leverages scientific and disciplined approaches to accelerate the global development of safe and effective medical therapeutics.