Associate Clinical Trial Manager (PhD) - Neuroscience / Ophthalmology
Pubblicato il 15-08-2026 - Medpace in Milano
ph3Job Summary /h3pMedpace is currently seeking candidates with PhDs and/or Post-Doctoral Research experience for a full-time, office-based Associate Clinical Trial Manager (aCTM) to join our Clinical Trial Management team. The aCTM will be a part of the Clinical Trial Management team working with Project Coordinators and Clinical Trial Managers in performance of clinical trial management activities. Candidate must have a desire to transfer and apply analytical and academic skills in clinical project administration and management. 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). /ph3Responsibilities /h3ulliCommunicate and collaborate on global study activities; working closely with the project coordinator and clinical trial manager /liliEnsure timely delivery of recurrent tasks consistently with a high degree of accuracyCompile and maintain project-specific status reports within the clinical trial management system /liliInteract with the internal project team, Sponsor, study sites, and third-party vendors /liliManage and perform quality control of our internal regulatory filing system /liliProvide oversight and management of study supplies /liliCreate and maintain project timelines /liliCoordinate project meetings and produce quality minutes.
/li /ulh3Qualifications /h3ulliPhD in Life Sciences /liliFluency in English with solid presentation skills /liliAbility to work in a fast-paced dynamic industry within an international team /liliPrior experience within the CRO or pharmaceutical industry not required but will be advantageous /li /ulh3Medpace Overview /h3pMedpace is a full-service clinical contract research organization (CRO) providing phase l-lV 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 the advancement of clinical research. We leverage in-country regulatory and therapeutic expertise across all major therapeutic areas including oncology, cardiology, metabolic, endocrinology, central nervous system, and anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, we employ more than 6,500 people across 40+ countries. /ph3Why Medpace? /h3pWhen you join Medpace, you become part of an innovative team that brings cutting-edge therapies to market while building a meaningful and rewarding career focused on scientific excellence and improving patient outcomes around the world through continuous learning and cross-functional collaboration. /ph3Purpose-Driven Work /h3pWork alongside physicians,
scientists, and industry-leading experts committed to advancing the global development of medical therapeutics through clinical research excellence /ph3Collaborative Culture /h3pContribute to an interactive team environment that empowers decision making, creative thinking, and continuous learning through open communication and mutual trust. /ph3Leadership throughout Medpace is both accessible and approachable /h3h3Continuous Growth Development /h3pOffice based environment with on-site mentors /ppDefined career paths with clear advancement opportunities /ppIndustry renowned onboarding and training programs designed to accelerate professional development /ppOngoing training and continuous learning opportunities throughout your career /ppAn environment that encourages employees to influence change, contribute ideas, and grow quickly /ph3Other Employee Benefits /h3ulliCompetitive compensation programs that recognize and reward performance /liliComprehensive health, wellness, retirement, and PTO benefits /liliOffice based culture with occasional WFH that provides flexibility for eligible positions after training /liliCompany-sponsored social events /liliPlease note benefits may vary based on country. /li /ulh3What to Expect Next /h3pA Medpace team member will review your application and if your profile matches our current needs, you will be contacted for an interview. While we review all applications carefully, we are unable to respond to every applicant, and only candidates selected for interviews will be contacted. /ph3Category: Clinical Trial Management /h3 /p #J-18808-Ljbffr