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Clinical Operations Lead H/F Excelya

Paris - 75
CDI
Bac +5
Industrie Pharmaceutique • Biotechn. • Chimie
Exp. 5 ans min.

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Les missions du poste

About the Job

Join Excelya, where Audacity, Care, and Energy define who we are and how we work. We believe in creating bold solutions and fostering an inclusive environment where collaboration and individual growth go hand in hand.

This role is an exciting opportunity to contribute to a dynamic, ambitious team in Clinical Operations. You will play a critical part in driving innovation and making an impact in the clinical research space, while enjoying a stimulating professional environment that encourages personal and intellectual growth.

Main Responsibilities

- Lead and coordinate the operational aspects of assigned clinical studies, including study start-up, site management, and monitoring activities to ensure compliance with protocols and GCP standards.
- Act as the primary liaison between project teams and clinical sites, ensuring effective communication and collaboration.
- Oversee the planning and execution of monitoring visits, including preparation of visit reports and follow-up on findings.
- Train and mentor Clinical Research Associates (CRAs) and ensure they are aligned with project goals and objectives.
- Review study-related documents for accuracy and completeness, ensuring regulatory compliance throughout the study lifecycle.
- Support the management of study budgets and timelines, providing regular updates to project stakeholders.
- Ensure that site staff are knowledgeable about study protocols and GCP requirements through ongoing training and support.
- Facilitate problem-solving and risk assessment to address issues that may arise during the study.

Le profil recherché

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

- Experience: Minimum of 5 years of experience in clinical monitoring and study management within a CRO or pharmaceutical company; prior experience as a CRA or in a lead role is highly desirable.
- Skills: Strong understanding of GCP, ICH guidelines, and regulatory requirements; excellent leadership, communication, and interpersonal skills; proficiency in using clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
- Education: Bachelor's degree in life sciences, medicine, or a related field; advanced degree is a plus.
- Languages: Bilingual in French, proficient in English; knowledge of additional languages is an advantage.

Bienvenue chez Excelya

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.

Publiée le 19/01/2026 - Réf : 1a3df509-3fe8-4955-bbc6-eaf5713ab6ab