Associate Clinical Trial Manager - PhD - Postdoctoral - Nephrology

Medpace; Irving (TX); On-site; USD 60,000 - 100,000; Full time

Job summary

An established industry player is seeking a dedicated Associate Clinical Trial Manager to join their Clinical Trial Management team. This role is perfect for recent PhD graduates in Life Sciences looking to transition into the pharmaceutical industry. You'll receive comprehensive training and work in a dynamic international environment, enhancing your career in clinical project management. The position involves collaboration with various stakeholders, ensuring project timelines are met, and maintaining high standards of quality control. If you're passionate about research and development of innovative therapeutics, this opportunity is for you.

Qualifications

• PhD in Life Sciences required.
• Ability to work in a dynamic international team.

Responsibilities

• Collaborate on global study activities with project teams.
• Ensure timely delivery of tasks with high accuracy.
• Manage study supplies and oversee project timelines.

Skills

Analytical Skills

Project Management

Communication

Education

PhD in Life Sciences

Job description

Associate Clinical Trial Manager - PhD - Postdoctoral - Nephrology

Medpace is currently seeking candidates with Nephrology-related PhDs and/or Post-Doctoral Research experience for a full-time, office-based Associate Clinical Trial Manager (aCTM). The aCTM is part of the Clinical Trial Management team working with Project Coordinators and Clinical Trial Managers in the performance of clinical trial management activities. Candidates 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 an intensive training period and demonstrate 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
• Manage study supplies and oversee project timelines
• Coordinate project meetings and produce quality minutes

Qualifications

• PhD in Life Sciences
• Ability to work in a fast-paced, dynamic industry within an international team
• Prior experience within the CRO or pharmaceutical industry is advantageous but not required