Early-Career Associate Clinical Trial Manager (Oncology)
Job SummaryMedpace is a leading CRO for Biotech companies and we are currently seeking candidates with PhDs and/or Post-Doctoral Research experience for a full-time Associate Clinical Trial Manager (aCTM) to join our Clinical Trial Management team in our Melbo…
Associate Clinical Trial Manager - PhD / Post-Doc (Oncology)
Job SummaryMedpace is a leading CRO for Biotech companies and we are currently seeking candidates with PhDs and/or Post-Doctoral Research experience for a full-time Associate Clinical Trial Manager (aCTM) to join our Clinical Trial Management team in our Melbo…
Director, Clinical Trial Management - CVRM (Cardiovascular/Renal/Metabolic)
Job SummaryMedpace is continuing to expand our global Clinical Trial Management team and is seeking an experienced Director, Clinical Trial Management (office base) to lead complex global clinical trials while developing and mentoring high-performing project m…
Director, Clinical Trial Management — Global CVRM Trials
Medpace, Inc. seeks an experienced Director of Clinical Trial Management (office-based) to lead complex global trials and mentor high-performing project management teams. This senior role emphasizes strategic leadership and execution in a fast-paced CRO enviro…
Advanced Clinical Practitioner - Haematology/Oncology Research
Medpace, Inc. seeks Advanced Clinical Practitioner/Nurse Practitioners with Haematology/Oncology experience to serve as clinical experts supporting study teams in clinical research (no direct patient care).You will work alongside physicians to review protocols…
Advanced Clinical Practitioner - Haematology / Oncology
Job SummaryWe are seekingAdvancedClinical Practitioner/Nurse Practitioners with Haematology/Oncology experiencewho are interested in being at the forefront of new treatments for patients with haematologic and oncologic diseases. This role will work side by sid…
Associate Director, Regulatory Submissions
Job SummaryWe are seeking a key manager to support the Medpace Study Start-up group in APAC Region while being office-based in Melbourne, Australia. This position will be an integral part of the Medpace clinical operations management team. This role will be re…
Global Regulatory Submissions Lead – Start-Up (Hybrid)
Medpace, Inc. seeks a Regulatory (Study Start Up) Submissions Manager for a full-time, office-based role in Melbourne, Australia. You will manage global start-up activities and ensure timely regulatory submissions to support clinical programs.Ideal candidates …
Clinical Site Partnerships Coordinator
Medpace is seeking a full-time, office-based Clinical Site Relationship Coordinator to join our Clinical Operations team in Melbourne, Australia. You will build and maintain relationships with site networks and support feasibility activities for pre- and post-…
Regulatory Submissions (Study Start-up) Manager
Job SummaryWe are currently seeking a full-time, office-based* Regulatory (Study Start Up) Submissions Manager to join our Clinical Operations team in Melbourne, Australia.ResponsibilitiesEfficiently manage and successfully execute all aspects of global start-…