Medpace is currently looking for Clinical Trial Manager (CTM) to lead global clinical research studies. This position is fully based in our Melbourne, Australia office. Medpace is a scientifically led organization involved in full services for our clients, giving the Medpace project teams the empowerment to truly lead and execute clinical trials.
ResponsibilitiesThe Clinical Trial Manager position performs project lead role for multiservice global clinical trials. The position interacts with sponsors and manages the timeline and project deliverables. This role coordinates for all services contracted for the study. CTMs are also responsible for leading cross functional team of clinical monitoring, study start-up, regulatory, contract, safety, medical monitoring etc. CTM may need to attend bid defense meetings and support business development team in winning new business.
Qualifications- Bachelor's degree in a health related field (Master's degree or Ph D is preferred);
- At least two years of clinical trial management experience in Asia Pacific region ideally in a CRO environment;
- Experience in Cardiovascular, Renal & Metabolic Disease (CVRM) studies required;
- Excellent communication skills including good written and spoken English; and
- Flexible, accountable and comfortable in working in a global environment.
People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today.
The work we've done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future.
What to Expect NextA Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.
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