Emplacement

Saint-Didier-au-Mont-d'Or
France
France

Contrat

À plein temps, Durée indéterminée

Date de publication:

2026-11-10

Online to:

2027-01-09
EUR 15.00 HOUR

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Associate Clinical Trial Manager (PhD) - Cardiovascular

Medpace
France
4 heures il y a

Job Summaryp p p Medpace is currently seeking candidates with strongCardiovascular related PhDs and/or Post-Doctoral Research experience /strong for a full-time, uoffice-based /u Associate Clinical Trial Manager (aCTM) to join our France, Lyon 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. /pp A fantastic opportunity for recent PhD graduates to enter the industry, receive solid foundational training, work in an international environment, and strongdevelop their career in the research and development of cutting-edge therapeutics /strong. 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 /p /pResponsibilitiesp p ulliCommunicate 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 accuracy /liliCompile 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 /liliProvide oversight and 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 /ul /p /pQualificationsp p ulliPhD 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 /ul /p /pMedpace Overviewp p p Medpace 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 /p /pWhy Medpace?p p p When 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. /pp emstrongPurpose-Driven Work /strong /em /pulli ulliWork alongside physicians, scientists, and industry-leading experts committed to advancing the global development of medical therapeutics through clinical research excellence /li /ul /li /ulp emstrongCollaborative Culture /strong /em /pulli ulliContribute to an interactive team environment that empowers decision making, creative thinking, and continuous learning through open communication and mutual trust. /liliLeadership throughout Medpace is both accessible and approachable /li /ul /li /ulp emstrongContinuous Growth Development /strong /em /pulli ulliOffice based environment with on-site mentors /liliDefined career paths with clear advancement opportunities /liliIndustry renowned onboarding and training programs designed to accelerate professional development /liliOngoing training and continuous learning opportunities throughout your career /liliAn environment that encourages employees to influence change, contribute ideas, and grow quickly /li /ul /li /ulp emstrongOther Employee Benefits /strong /em /pulli ulliCompetitive 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 /li /ul /li /ulp emPlease note benefits may vary based on country. /em /pp strongWhat to Expect Next /strong /pp A 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 /ph3Job Summary /h3ullistrongCategory: /strongClinical Trial Management /li /ul

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Associate Clinical Trial Manager (PhD) - Cardiovascular

Emplacement

Contrat

Date de publication:

Online to:

Associate Clinical Trial Manager (PhD) - Cardiovascular

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