Clinical Trial Manager H/F Excelya
- Paris - 75
- CDI
- Bac +5
- Industrie Pharmaceutique • Biotechn. • Chimie
Les missions du poste
AbouttheJob
JoinExcelya,whereAudacity,Care,andEnergydefinewhoweareandhowwework.Webelieveincreatingboldsolutionsandfosteringaninclusiveenvironmentwherecollaborationandindividualgrowthgohandinhand.
Thisroleisanexcitingopportunitytocontributetoadynamic,ambitiousteam.Youwillplayacriticalpartindrivinginnovationandmakinganimpactintheclinicalresearchspace,whileenjoyingastimulatingprofessionalenvironmentthatencouragespersonalandintellectualgrowth.
Main Responsibilities
- Lead the planning, setup, and coordination of national clinical studies, ensuring timelines, quality, and compliance are met.
- Conduct feasibility assessments when required, including expert contacts and cross-functional meetings.
- Oversee CTIS submissions and ensure all regulatory deliverables are submitted within deadlines.
- Supervise or contribute to the development and validation of study documentation, ensuring alignment with company SOPs and local regulations.
- Maintain and update study tracking tools and dashboards for project oversight.
- Act as the main interface between project stakeholders, preferred provider monitoring teams, and administrative support; organize progress meetings and ensure follow-up actions.
- Monitor patient recruitment, site engagement, and risk management, implementing mitigation plans as needed.
- Manage study budgets, from financial planning to tracking and variance justification, and oversee database lock and study closure activities.
WhyJoinUs?
AtExcelya,wecombinepassionforsciencewithenthusiasmforteamworktoredefineexcellenceinhealthcare.
Here'swhatmakesusunique-
Weareayoung,ambitioushealthcompanyrepresenting900Excelyates,driventobecomeEurope'sleadingmid-sizeCROwiththebestemployeeexperience.Ourone-stopproviderservicemodel-offeringfull-service,functionalserviceprovider,andconsulting-enablesyoutoevolvethroughdiverseprojects.Workingalongsidepreeminentexperts,youwillhelpimprovescientific,operational,andhumanknowledgetoenhancethepatient'sjourney.
Excellingwithcaremeansbenefitingfromanenvironmentthatvaluesyournaturaltalents,pushesboundarieswithaudacity,andnurturesyourpotential,allowingyoutocontributefullytooursharedmission.
About You
At Excelya, taking audacious steps is encouraged, so we're looking for individuals who are ready to grow with us and share our values.
- Experience:Proven ability to thrive in collaborative, fast-moving environments (no minimum years required-talent matters most to us!).
- Skills:Experience in clinical project management within pharma, biotech, or CRO. Proven skills in budget management, risk assessment, and cross-functional coordination at a local level.
- Education:Degree in Life Sciences or Pharmacy (Master's or equivalent).
- Languages:French & English mandatory
Excelya is an independent partner that serves Biotech, Pharma, and Medical Device organizations with a comprehensive range of full-service CRO, FSP, and Resourcing solutions guided by our values Energy, Care and Audacity.
Founded in 2014 and headquartered in Paris, France, Excelya has a global team of 900+ experts who understand the critical needs of clients to provide bespoke and robust trial solutions across a broad spectrum of therapeutic areas.
We take a one-team approach to work: our shared success is the result of collaboration at every stage of a project, from regulatory affairs and clinical operations to quality assurance and strategic development.
Excelya is committed to helping our clients deliver life-changing therapies collaboratively, so we can transform tomorrow together.
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Publiée le 10/10/2025 - Réf : dbdb4b78-6bab-42db-94d3-ffc1ceb8b6be
Clinical Trial Manager H/F
- Paris - 75
- CDI
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