Job Summary
Medpace is currently seeking candidates with PhDs and/or Post-Doctoral Research experience in nuclear medicine/radiopharmaceuticals/radiation oncology for a full-time Associate Clinical Trial Manager (aCTM) to join our Clinical Trial Management team in Melbourne, Australia. The aCTM will be 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.
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 radiopharmaceuticals. 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.
* Coordinate project meetings and produce quality minutes.
Qualifications
* PhD in Life Sciences (nuclear medicine/radiopharmaceuticals/radiation oncology or related).
* 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 is not required but will be advantageous.
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