Associate Clinical Trial Manager - PhD - Metabolic

Medpace; Cincinnati (OH); On-site; USD 65,000 - 95,000; Full time

Job summary

An innovative CRO is seeking a dynamic Associate Clinical Trial Manager with a PhD in Life Sciences to join their Clinical Trial Management team. This role offers a unique opportunity for recent graduates to transition into the industry, providing foundational training and an accelerated career path in clinical project management. You will engage in global study activities, ensuring tasks are delivered with precision and collaborating with diverse teams. If you are eager to apply your analytical skills in a fast-paced, international environment and contribute to cutting-edge therapeutics research, this position is perfect for you.

Qualifications

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

Responsibilities

• Collaborate on global study activities with the project team.
• Maintain project status reports and manage project timelines.
• Coordinate meetings and interact with internal teams and sponsors.

Skills

Analytical Skills

Communication Skills

Organizational Skills

Presentation Skills

Education

PhD in Life Sciences

Job description

Associate Clinical Trial Manager - PhD - Metabolic

Medpace is a leading CRO for Biotech companies and we are currently seeking candidates with PhDs and/or Post-Doctoral Research experience within Metabolic research 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 and apply analytical and academic skills in clinical project administration and management.

This is a great opportunity for recent PhD graduates to enter the industry, receive foundational training, work internationally, and develop their careers in cutting-edge therapeutics research. Expect an intensive training period and an accelerated career path into Clinical Trial Management.

Responsibilities

1. Communicate and collaborate on global study activities with the project team;
2. Ensure timely delivery of tasks with high accuracy;
3. Maintain project status reports within the clinical trial management system;
4. Interact with internal teams, sponsors, study sites, and vendors;
5. Oversee regulatory filing systems and study supplies;
6. Create and manage project timelines;
7. Coordinate meetings and produce minutes.

Qualifications

• PhD in Life Sciences;
• Fluency in English with strong presentation skills;
• Ability to work in a fast-paced, international environment;
• Experience in CRO or pharmaceutical industry is advantageous but not required;
• Excellent computer, organizational, and communication skills.