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Job Title


Associate Clinical Trial Manager - PhD / Post-Doc ((Cardiovascular, Renal & Meta


Company : Medpace


Location : Melbourne, Australia


Created : 2025-07-03


Job Type : Full Time


Job Description

Associate Clinical Trial Manager - PhD / Post-Doc ((Cardiovascular, Renal & Metabolic Disease (CVRM))Join to apply for the Associate Clinical Trial Manager - PhD / Post-Doc ((Cardiovascular, Renal & Metabolic Disease (CVRM)) role at MedpaceContinue with Google Continue with GoogleAssociate Clinical Trial Manager - PhD / Post-Doc ((Cardiovascular, Renal & Metabolic Disease (CVRM))Join to apply for the Associate Clinical Trial Manager - PhD / Post-Doc ((Cardiovascular, Renal & Metabolic Disease (CVRM)) role at MedpaceMedpace 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 Melbourne, Australia office. The aCTM will be a part of the Clinical Trial Management team and support Project Coordinators and Clinical Trial Managers in performance of project management activities. Candidate 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 PhD 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).ResponsibilitiesCommunicate 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; andCoordinate project meetings and produce quality minutes.QualificationsPhD 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; andExcellent computer (word-processing, databases, Excel, Windows), organisational, and communication skills.Medpace OverviewMedpace is a full-service clinical contract research organization (CRO). We provide 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 its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries.Why Medpace?People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today.The work weve 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.Medpace PerksFlexible work environmentCompetitive compensation and benefits packageCompetitive PTO packagesStructured career paths with opportunities for professional growthCompany-sponsored employee appreciation eventsEmployee health and wellness initiativesAwardsRecognized by Forbes as one of America''s Most Successful Midsize Companies in 2021, 2022, 2023 and 2024Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibilityWhat To Expect NextA Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.Seniority levelSeniority levelNot ApplicableEmployment typeEmployment typeFull-timeJob functionJob functionResearch, Analyst, and Information TechnologyIndustriesPharmaceutical ManufacturingReferrals increase your chances of interviewing at Medpace by 2xContinue with Google Continue with GoogleMelbourne, Victoria, Australia A$130,000 - A$160,000 3 weeks agoMelbourne, Victoria, Australia 2 weeks agoSouth Yarra, Victoria, Australia 1 week agoAssociate Director, Clinical Trial ManagerMelbourne, Victoria, Australia 2 weeks agoClinical Trial Manager (Neuroscience/CNS)South Yarra, Victoria, Australia 2 weeks agoAssociate Clinical Trial Manager - PhD / Post-Doc - Infectious DiseaseSouth Yarra, Victoria, Australia 1 week agoAssociate Clinical Trial Manager - PhD / Post-Doc (Oncology)South Yarra, Victoria, Australia 1 week agoClinical Trial Manager ((Cardiovascular, Renal & Metabolic Disease (CVRM))South Yarra, Victoria, Australia 1 day agoMelbourne, Victoria, AustraliaA$118,771.00-A$128,556.001 week agoAssociate Clinical Trial Manager (PhD, nuclear medicine / radiopharmaceuticals / radiation oncology)South Yarra, Victoria, Australia 1 week agoMelbourne, Victoria, Australia 3 days agoMelbourne, Victoria, AustraliaA$110,000.00-A$125,000.002 weeks agoSouth Yarra, Victoria, Australia 1 day agoInhouse Clinical Research Associate - AustraliaMelbourne, Victoria, Australia 1 week agoMelbourne, Victoria, AustraliaA$85,000.00-A$135,000.005 hours agoMelbourne, Victoria, Australia 14 hours agoMelbourne, Victoria, AustraliaA$100,000.00-A$120,000.001 week agoMelbourne, Victoria, AustraliaA$100,000.00-A$140,000.001 month agoMelbourne, Victoria, Australia 3 weeks agoSenior Clinical Research Associate (CRA) CROMelbourne, Victoria, Australia 11 hours agoClinical Research Associate II, Melbourne basedRegulatory Start Up Associate II - AustraliaMelbourne, Victoria, Australia 1 week agoMelbourne, Victoria, Australia 2 weeks agoSouth Yarra, Victoria, Australia 2 weeks agoMelbourne, Victoria, Australia 5 days agoMelbourne, Victoria, Australia 3 weeks agoMelbourne, Victoria, Australia A$80,000 - A$130,000 1 week agoClinical Research Associate II/ Senior Clinical Research AssociateMelbourne, Victoria, Australia 2 days agoMelbourne, Victoria, Australia 6 days agoSenior Clinical Research Associate I (SCRA1), FSP modelMelbourne, Victoria, Australia 2 weeks agoMelbourne, Victoria, Australia 2 weeks agoMelbourne, Victoria, Australia 2 weeks agoWere unlocking community knowledge in a new way. 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