Medpace is a leading CRO for Biotech companies and we are currently seeking candidates with Ph Ds and/or Post-Doctoral Research experience for a full-time Associate Clinical Trial Manager (a CTM) to join our Clinical Trial Management team in our Melbourne, Australia office. The a CTM 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 fantastic opportunity for recent Ph D 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.
- Ph D in Life Sciences;
- Experienced in Cardiovascular, Renal & Metabolic Disease (CVRM);
- 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), organisational, and communication skills.