Associate Clinical Trial Manager

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 Medpace Continue with Google Continue with Google 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 Medpace Medpace 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; and Coordinate 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; and Excellent 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 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.Medpace PerksFlexible work environment Competitive compensation and benefits package Competitive PTO packages Structured career paths with opportunities for professional growth Company-sponsored employee appreciation events Employee health and wellness initiatives AwardsRecognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024 Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility What To Expect NextA Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps. Seniority level Seniority level Not Applicable Employment type Employment type Full-time Job function Job function Research, Analyst, and Information Technology Industries Pharmaceutical Manufacturing Referrals increase your chances of interviewing at Medpace by 2x Continue with Google Continue with Google Melbourne, Victoria, Australia A$130,000 - A$160,000 3 weeks ago Melbourne, Victoria, Australia 2 weeks ago South Yarra, Victoria, Australia 1 week ago Associate Director, Clinical Trial Manager Melbourne, Victoria, Australia 2 weeks ago Clinical Trial Manager (Neuroscience/CNS) South Yarra, Victoria, Australia 2 weeks ago Associate Clinical Trial Manager - PhD / Post-Doc - Infectious Disease South Yarra, Victoria, Australia 1 week ago Associate Clinical Trial Manager - PhD / Post-Doc (Oncology) South Yarra, Victoria, Australia 1 week ago Clinical Trial Manager ((Cardiovascular, Renal & Metabolic Disease (CVRM)) South Yarra, Victoria, Australia 1 day ago Melbourne, Victoria, AustraliaA$118,771.00-A$128,556.001 week ago Associate Clinical Trial Manager (PhD, nuclear medicine / radiopharmaceuticals / radiation oncology) South Yarra, Victoria, Australia 1 week ago Melbourne, Victoria, Australia 3 days ago Melbourne, Victoria, AustraliaA$110,000.00-A$125,000.002 weeks ago South Yarra, Victoria, Australia 1 day ago Inhouse Clinical Research Associate - Australia Melbourne, Victoria, Australia 1 week ago Melbourne, Victoria, AustraliaA$85,000.00-A$135,000.005 hours ago Melbourne, Victoria, Australia 14 hours ago Melbourne, Victoria, AustraliaA$100,000.00-A$120,000.001 week ago Melbourne, Victoria, AustraliaA$100,000.00-A$140,000.001 month ago Melbourne, Victoria, Australia 3 weeks ago Senior Clinical Research Associate (CRA) CRO Melbourne, Victoria, Australia 11 hours ago Clinical Research Associate II, Melbourne based Regulatory Start Up Associate II - Australia Melbourne, Victoria, Australia 1 week ago Melbourne, Victoria, Australia 2 weeks ago South Yarra, Victoria, Australia 2 weeks ago Melbourne, Victoria, Australia 5 days ago Melbourne, Victoria, Australia 3 weeks ago Melbourne, Victoria, Australia A$80,000 - A$130,000 1 week ago Clinical Research Associate II/ Senior Clinical Research Associate Melbourne, Victoria, Australia 2 days ago Melbourne, Victoria, Australia 6 days ago Senior Clinical Research Associate I (SCRA1), FSP model Melbourne, Victoria, Australia 2 weeks ago Melbourne, Victoria, Australia 2 weeks ago Melbourne, Victoria, Australia 2 weeks ago We’re unlocking community knowledge in a new way. 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