ph3Job Summary /h3 pMedpace is currently seeking candidates with bPhDs and/or Post-Doctoral Research experience /b 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. /p pA fantastic opportunity for recent PhD graduates to enter the industry, receive solid foundational training, work in an international environment, and bdevelop their career in the research and development of cutting-edge therapeutics /b. 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). /p h3Responsibilities /h3 ul liCommunicate and collaborate on global study activities; working closely with the project coordinator and clinical trial manager /li liEnsure timely delivery of recurrent tasks consistently with a high degree of accuracy /li liCompile and maintain project-specific status reports within the clinical trial management system /li liInteract with the internal project team, Sponsor, study sites,



and third-party vendors /li liManage and perform quality control of our internal regulatory filing system /li liProvide oversight and management of study supplies /li liCreate and maintain project timelines /li liCoordinate project meetings and produce quality minutes /li /ul h3Qualifications /h3 ul liPhD in Life Sciences /li liFluency in English with solid presentation skills /li liAbility to work in a fast-paced dynamic industry within an international team /li liPrior experience within the CRO or pharmaceutical industry not required but will be advantageous /li /ul h3Medpace Overview /h3 pMedpace 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. /p h3Why Medpace? /h3 pWhen 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. /p pbPurpose-Driven Work /b /p ul liWork alongside physicians, scientists,



and industry-leading experts committed to advancing the global development of medical therapeutics through clinical research excellence /li /ul pbCollaborative Culture /b /p ul liContribute to an interactive team environment that empowers decision making, creative thinking, and continuous learning through open communication and mutual trust. /li liLeadership throughout Medpace is both accessible and approachable /li /ul pbContinuous Growth Development /b /p ul liOffice based environment with on-site mentors /li liDefined career paths with clear advancement opportunities /li liIndustry renowned onboarding and training programs designed to accelerate professional development /li liOngoing training and continuous learning opportunities throughout your career /li liAn environment that encourages employees to influence change, contribute ideas, and grow quickly /li /ul pbOther Employee Benefits /b /p ul liCompetitive compensation programs that recognize and reward performance /li liComprehensive health, wellness, retirement, and PTO benefits /li liOffice based culture with occasional WFH that provides flexibility for eligible positions after training /li liCompany-sponsored social events /li /ul pPlease note benefits may vary based on country. /p h3What to Expect Next /h3 pA 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. /p /p #J-18808-Ljbffr

📌 Associate Clinical Trial Manager (PhD) - Neuroscience / Ophthalmology (Ravello)
🏢 Medpace
📍 Ravello