Associate Clinical Trial Manager - PhD / Post-Doc Experience - Cincinnati, OH

Medpace; Cincinnati (OH); On-site; USD 60,000 - 100,000; Full time

Job summary

An established industry player is seeking a motivated Associate Clinical Trial Manager to join their Clinical Trial Management team in Cincinnati. This full-time, office-based role is perfect for recent PhD graduates looking to transition into the biotech industry. You will receive comprehensive training and gain hands-on experience in managing clinical trials. The position offers an exciting opportunity to work in a dynamic, international environment, collaborating with various stakeholders to ensure the success of clinical projects. If you're ready to leverage your analytical skills and drive your career forward, this role is for you.

Qualifications

• PhD in Life Sciences required for the role.
• Strong communication and organizational skills are essential.

Responsibilities

• Communicate and collaborate on global study activities with project teams.
• Create and manage project timelines effectively.

Skills

Analytical Skills

Project Management

Communication Skills

Organizational Skills

Education

PhD in Life Sciences

Tools

Microsoft Word

Microsoft Excel

Databases

Windows OS

Job description

Associate Clinical Trial Manager - PhD / Post-Doc Experience - Cincinnati, OH

Medpace is a leading CRO for Biotech companies and we are currently seeking candidates with PhDs and/or Post-Doctoral Research experience for a full-time, office-based Associate Clinical Trial Manager (aCTM) to join our Clinical Trial Management team. The aCTM will support Project Coordinators and Clinical Trial Managers in project management activities. Candidates must have a desire to transfer analytical and academic skills into clinical project administration and management.

This is an excellent opportunity for recent PhD graduates to enter the industry, receive comprehensive training, work in an international environment, and develop their careers in cutting-edge therapeutics research. Candidates should expect an intensive training period and demonstrate the motivation for an accelerated career path into Clinical Trial Management (CTM).

Responsibilities

• Communicate and collaborate on global study activities with project teams, sponsors, study sites, and vendors.
• Ensure timely and accurate completion of recurring tasks.
• Maintain project-specific status reports in the clinical trial management system.
• Oversee internal regulatory filings and study supplies.
• Create and manage project timelines.
• Coordinate project meetings and prepare minutes.

Qualifications

• PhD in Life Sciences.
• Fluency in English with strong presentation skills.
• Ability to work in a fast-paced, international environment.
• Prior CRO or pharmaceutical industry experience is advantageous but not required.
• Proficient in computer skills including Word, Excel, databases, and Windows; excellent organizational and communication skills.