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Associate Clinical Trial Manager - Phd / Post-doc (cardiovascular, Renal & Metabolic Disease (cvrm),

Last update 2025-02-15
Expires 2025-03-15
ID #2497318803
Free
Associate Clinical Trial Manager - Phd / Post-doc (cardiovascular, Renal & Metabolic Disease (cvrm),
Australia, Melbourne, Melbourne,
Modified December 10, 2024

Description

Job Summary

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.
Qualifications
  • 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.

Job details:

Job type: Full time
Contract type: Permanent
Salary type: Per annum
Occupation: Associate clinical trial manager - phd / post-doc (cardiovascular, renal & metabolic disease (cvrm)

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