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CRA Manager

Excelya Group

Paris

Sur place

EUR 60 000 - 80 000

Plein temps

Il y a 18 jours

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Résumé du poste

A leading clinical research organization is seeking an experienced Clinical Research Associate (CRA) Manager to lead a team of CRAs in Paris. You will oversee clinical trial activities, ensure compliance with regulatory requirements, and foster a culture of excellence. Ideal candidates have at least 5 years of monitoring experience, with 2 years in a managerial role, and must be fluent in both English and French. Join us to contribute to innovative healthcare solutions in a supportive environment.

Prestations

Encouragement for professional growth
A culture of collaboration and excellence

Qualifications

  • Minimum of 5 years of experience in clinical monitoring.
  • At least 2 years in a supervisory or managerial role.
  • Proficiency in English and French (both written and spoken).

Responsabilités

  • Lead and manage a team of CRAs, providing guidance and support.
  • Ensure compliance with ICH-GCP guidelines and regulations.
  • Collaborate with teams to develop study strategies and manage timelines.
  • Conduct regular team meetings and performance evaluations.
  • Maintain oversight of study sites for data integrity.
  • Drive process improvements and implement best practices.
  • Assist in the recruitment and onboarding of new team members.

Connaissances

Leadership skills
Understanding of ICH-GCP guidelines
Motivation and mentoring

Formation

Master's degree in Life Sciences
Description du poste
About the Job

JoinExcelya, whereAudacity, Care, and Energydefinewhoweareandhowwework.Webelieveincreatingboldsolutionsandfosteringaninclusiveenvironmentwherecollaborationandindividualgrowthgohandinhand.

We are seeking a highly motivated and experienced Clinical Research Associate (CRA) Manager to lead our dedicated team of CRAs. In this role, you will be responsible for overseeing clinical trial activities and ensuring compliance with regulatory requirements while fostering a culture of excellence and collaboration within the team.

Main Responsibilities
  • Lead and manage a team of CRAs, providing guidance, coaching, and support in their professional development.
  • Ensure that clinical trial monitoring and related activities are performed in compliance with ICH-GCP guidelines, SOPs, and applicable regulations.
  • Collaborate with cross‑functional teams to develop study strategies, manage timelines, and ensure project milestones are met.
  • Conduct regular team meetings and performance evaluations, fostering an open environment for feedback and continuous improvement.
  • Maintain an oversight of study sites, ensuring adherence to protocols and data integrity, while actively resolving any issues related to site performance.
  • Drive process improvements and implement best practices that improve operational efficiency and quality in clinical monitoring activities.
  • Assist in the recruitment and onboarding of new team members, ensuring alignment with Excelya’s culture and values.
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: Minimum of 5 years of experience in clinical monitoring with at least 2 years in a supervisory or managerial role.
  • Skills: Strong understanding of ICH‑GCP guidelines and regulations governing clinical trials, exceptional leadership skills, and the ability to motivate and mentor team members.
  • Education: Master's degree in Life Sciences or related field; advanced degree (Master's or equivalent) is a plus.
  • Languages: Proficiency in English and French (both written and spoken).
WhyJoinUs?

At Excelya,wecombinepassionforsciencewithenthusiasmforteamworktoredefineexcellenceinhealthcare.

Here'swhatmakesusunique.

Weareayoung,ambitioushealthcompanyrepresenting900Excelyates,driventobecomeEurope'sleadingmid-sizeCROwiththebestemployeeexperience.Ourone-stopproviderservicemodelofferingfull-service,functionalserviceprovider,andconsultingenablesyoutoevolvethroughdiverseprojects.Workingalongsidepreeminentexperts,youwillhelpimprovescientific,operational,andhumanknowledgetoenhancethepatient'sjourney.

Excellingwithcaremeansbenefitingfromanenvironmentthatvaluesyournaturaltalents,pushesboundarieswithaudacity,andnurturesyourpotential,allowingyoutocontributefullytooursharedmission.

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