Associate Clinical Trial Manager - Cincinnati, OH

Medpace; Cincinnati (OH); On-site; USD 70,000 - 90,000; Full time

Job summary

Medpace is seeking an Associate Clinical Trial Manager (aCTM) to join our Clinical Trial Management team. This office-based role in Cincinnati supports Project Coordinators and Clinical Trial Managers, applying analytical and academic skills to clinical project administration and management.

This is an excellent entry point for PhD graduates to enter the industry, with intensive training and rapid career development in a global R&D environment.

Qualifications

• PhD in Life Sciences is required.

Responsibilities

• Communicate and collaborate on global study activities; work closely with the project coordinator and clinical trial manager.

Skills

Fluency in English

Presentation skills

Computer skills

Cross-functional collaboration

Education

PhD in Life Sciences

Job description

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 be a part of the Clinical Trial Management team and support Project Coordinators and Clinical Trial Managers in performance of project management activities. Candidate must have a desire to transfer and apply analytical and academic skills in clinical project administration and management.

This is a fantastic opportunity for recent PhD graduates to enter the industry, receive solid foundational training, work in an international environment, and develop their career in the research and development of cutting-edge therapeutics. Candidates should expect to have an intensive training period and show the desire and aptitude for an accelerated career path into Clinical Trial Management (CTM).

Responsibilities

• Communicate and collaborate on global study activities; working closely with the project coordinator and clinical trial manager;
• Ensure timely delivery of recurrent tasks consistently with a high degree of accuracy;
• Compile and maintain project-specific status reports within the clinical trial management system;
• Interact with the internal project team, Sponsor, study sites, and third-party vendors;
• Provide oversight and quality control of our internal regulatory filing system;
• Provide oversight and management of study supplies;
• Create and maintain project timelines; and
• Coordinate project meetings and produce quality minutes.

Qualifications

• PhD in Life Sciences;
• Fluency in English with solid presentation skills;
• Ability to work in a fast-paced dynamic industry within an international team;
• Prior experience within the CRO or pharmaceutical industry not required but will be advantageous; and
• Excellent computer (word-processing, databases, Excel, Windows), organizational, and communication skills.