Job Summary
Medpace is a leading Contract Research Organization (CRO) for biotech companies. We are seeking candidates with PhDs and/or Post-Doctoral Research experience to join our Clinical Trial Management team in Melbourne, Australia.
This role offers recent PhD graduates the opportunity to enter the industry, receive solid foundational training, work in an international environment, and develop their career in clinical project administration and management.
Responsibilities
* Communicate and collaborate on global study activities;
* Ensure timely delivery of recurrent tasks consistently with high accuracy;
* Compile and maintain project-specific status reports within the clinical trial management system;
* Interact with internal teams, sponsors, study sites, and third-party vendors;
* Provide oversight and quality control of our regulatory filing system;
* Manage study supplies;
* Create and maintain project timelines;
* Coordinate project meetings and produce minutes.
Requirements
* PhD in Life Sciences;
* Experience in Cardiovascular, Renal & Metabolic Disease;
* Fluency in English with strong presentation skills;
* Ability to work in a fast-paced dynamic industry within an international team;
* Prior experience in CRO or pharmaceutical industry is advantageous; and
* Excellent computer, organizational, and communication skills.
About Medpace
We are a full-service CRO providing Phase I-IV clinical development services to the biotechnology, pharmaceutical, and medical device industries.
Our mission is to accelerate the global development of safe and effective medical therapeutics through our scientific and disciplined approach.
We leverage local expertise across all major therapeutic areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral, and anti-infective.
Why Medpace?
Career Development Opportunities. Competitive Compensation and Benefits Package. Flexible Work Environment. Collaborative Team Culture.