Radiopharmaceuticals CTM Associate — Global Clinical Trials

Medpace; Cincinnati (OH); Sur place; GBP 42 000 - 62 000; Plein temps

Avantages offerts par ce poste

Flexible work environment

Competitive compensation and benefits

Competitive PTO packages

Structured career paths

Company-sponsored appreciation events

Employee health and wellness

Forbes recognition awards

Résumé du poste

Medpace is seeking candidates with PhDs and/or Post-Doctoral Research experience in nuclear medicine, medical physics, medical imaging or radiopharmaceuticals for a full-time, office-based Associate Clinical Trial Manager to join our Clinical Trial Management team. The aCTM will work with Project Coordinators and Clinical Trial Managers in performance of clinical trial management activities.

A fantastic opportunity for recent PhD graduates to enter the industry, receive solid foundational

Qualifications

• PhD or Post-Doc in Radiopharmaceuticals, nuclear medicine, medical imaging or related field.
• Fluency in English with solid presentation skills.
• Ability to work in a fast-paced dynamic industry within an international team.
• Prior CRO or pharmaceutical industry experience is advantageous.

Responsabilités

• Communicate and collaborate on global study activities with the Project Coordinator and Clinical Trial Manager.
• Ensure timely delivery of recurrent tasks with high accuracy.
• Compile and maintain project-specific status reports within the clinical trial management system.
• Interact with internal project team, Sponsor, study sites, and third-party vendors.
• Provide oversight of the internal regulatory filing system.
• Provide oversight and management of study supplies.
• Create and maintain project timelines.
• Coordinate project meetings and produce quality minutes.

Connaissances

Fluency in English

Formation

PhD/Post-Doc

Description du poste

Medpace is seeking candidates with PhDs and/or Post-Doctoral Research experience in nuclear medicine, medical physics, medical imaging or radiopharmaceuticals for a full-time, office-based Associate Clinical Trial Manager to join our Clinical Trial Management team. The aCTM will work with Project Coordinators and Clinical Trial Managers in performance of clinical trial management activities.

A fantastic opportunity for recent PhD graduates to enter the industry, receive solid foundational