Senior Oncology CRA I – Home-Based (Paris Area)

Syneos Health France SARL

France

Hybride

EUR 42 000 - 54 000

Plein temps

Il y a 3 jours
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Résumé du poste

Syneos Health France SARL is seeking a Senior CRA I in Oncology to support sponsor-dedicated studies from a home-based role in the Paris area. You will monitor trial sites, ensure GCP compliance, and collaborate with the global clinical operations team.

Responsibilities include site qualification and initiation visits, interim monitoring, data verification, query resolution, and facilitating regulatory documentation. Travel up to 75% may be required.

Qualifications

  • Bachelor’s degree or RN in a related field or equivalent combination of education, training and experience.
  • Knowledge of Good Clinical Practice/ICH Guidelines and other applicable regulatory requirements.
  • Excellent communication, presentation and interpersonal skills. Basic level of critical thinking skills expected.
  • Ability to manage required travel of up to 75% on a regular basis

Responsabilités

  • Perform site qualification, site initiation, interim monitoring, site management and close-out visits (on-site or remote).
  • Ensure regulatory, ICH-GCP and GPP compliance and protocol adherence.
  • Maintain ISF/TMF alignment and accurate source data verification.
  • Conduct data reviews, query resolution, and IP inventory as applicable.
  • Support recruitment, retention and site collaboration with project teams.
  • Provide training or mentorship to junior CRAs as needed.

Connaissances

GCP knowledge
Communication skills
Travel readiness

Formation

Bachelor’s degree or RN

Description du poste

Syneos Health France SARL is seeking a Senior CRA I in Oncology to support sponsor-dedicated studies from a home-based role in the Paris area. You will monitor trial sites, ensure GCP compliance, and collaborate with the global clinical operations team.

Responsibilities include site qualification and initiation visits, interim monitoring, data verification, query resolution, and facilitating regulatory documentation. Travel up to 75% may be required.

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