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
• Expertise related to obesity, diabetes, MASH, MAFLD, hypoglycemia, or rare endocrine and metabolic diseases
• Fluency in English with solid presentation skills
• Strong organizational, communication, and computer skills (Excel, databases, etc.)
• Ability to work in a fast-paced, dynamic, and international environment

Preferred Qualifications

• Prior experience within the CRO or pharmaceutical industry

Benefits

• Competitive salary range ($70,000 - $90,000) with potential for bonus and equity awards
• Comprehensive medical, dental, and vision insurance
• 401(k) and various savings accounts (HSA/FSA)
• Paid vacation, sick days, and holidays
• Work from home flexibility
• Disability and life insurance, including pet insurance
• Travel expense reimbursement

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, Medpace employs over 6,000 people across 40+ countries, leveraging therapeutic expertise to accelerate the global development of safe and effective medical therapeutics.