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Date de publication:

2026-09-22

Online to:

2026-11-21
EUR 15.00 HOUR

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Experienced Clinical Research Associate

Medpace
France
4 heures il y a

Job SummaryOur clinical activities are growing rapidly, and we are currently seeking an Experienced Clinical Research Associate to join our Clinical/ Country Operations team in France. This position will work on a team to accomplish tasks and projects that are instrumental to the company’s success. If you want an exciting career where you use your previous expertise and can develop and grow your career even further, then this is the opportunity for you. We offer the following:Customized Fast PACE CRA training program based on your experience and therapeutic background and interestUser friendly CTMS with electronic submission and approval of monitoring visit reportsOngoing therapeutic training by our in-house physicians who are medical and regulatory expertsNational assignments with a very large pipeline of projects possibility Close collaboration with CRA managerOpportunities to work with international project team Competitive travel bonusNo metric for minimum required days on site per monthOpportunity for transversal activity like CRA lead positions, mentoring, CRA evaluator, super users, SME role.Possibility to be home based in various locations in France.ResponsibilitiesCompletion of monitoring reports and follow-up letters.Conduction of qualification, initiation, monitoring, and closeout visits for research sites in compliance with the approved protocolCommunication with the medical site staffEnsure good documentation practices are being adhered to and communicating protocol deviations appropriately per SOPs, GCP and applicable regulatory requirementsRegulatory document reviewVerification and review of adverse events, serious adverse events, concomitant medications and corresponding illnesses to confirm accurate data reporting in accordance with the protocolAssessing the clinical research site’s patient recruitment and retention success and offering suggestions for improvementCompletion of monitoring reports and follow-up letters, which includes providing summaries of the significant findings, deviations, deficiencies, and recommended actions to secure complianceQualificationsExperience as a Clinical Research Associate;Approximately 60-80% non-local, national travel is required;Must have a minimum of a bachelor’s degree in a health or science related field;Proficient knowledge of Microsoft Office;Fluency in French English; Outstanding communication skills; andMust be detail-oriented and efficient in time management.Medpace OverviewMedpace 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.Why Medpace?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.Purpose-Driven WorkWork alongside physicians, scientists, and industry-leading experts committed to advancing the global development of medical therapeutics through clinical research excellenceCollaborative CultureContribute to an interactive team environment that empowers decision making, creative thinking, and continuous learning through open communication and mutual trust.Leadership throughout Medpace is both accessible and approachableContinuous Growth DevelopmentOffice based environment with on-site mentorsDefined career paths with clear advancement opportunitiesIndustry renowned onboarding and training programs designed to accelerate professional developmentOngoing training and continuous learning opportunities throughout your careerAn environment that encourages employees to influence change, contribute ideas, and grow quicklyOther Employee BenefitsCompetitive compensation programs that recognize and reward performanceComprehensive health, wellness, retirement, and PTO benefitsOffice based culture with occasional WFH that provides flexibility for eligible positions after trainingCompany-sponsored social events Please note benefits may vary based on country. What to Expect NextA 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.Job SummaryCategory: Clinical Research Associate

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Experienced Clinical Research Associate

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Experienced Clinical Research Associate

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