Oncology CRA I: Remote Monitoring & Site Mgmt (Paris)

Syneos Health, Inc.; Paris; Hybride; EUR 55 000 - 70 000; Plein temps

Résumé du poste

Syneos Health, Inc. is recruiting a CRA I in Oncology based in the Paris area to monitor sites, ensure GCP compliance, and support trial execution for sponsor-dedicated projects. You will collaborate with cross-functional teams, manage site relationships, and travel up to 75% as required.

The role emphasizes regulatory knowledge, data integrity, and proactive site management to deliver high-quality trial results in a fast-paced environment.

Qualifications

• Bachelor’s degree or RN in a related field; equivalent combinations of education and experience accepted.
• Knowledge of Good Clinical Practice/ICH Guidelines and applicable regulatory requirements.
• Excellent communication, presentation and interpersonal skills.
• Strong computer skills and adaptability to new technologies.
• Willingness to travel up to 75% on a regular basis.

Responsabilités

• Performs site qualification, initiation, interim monitoring, site management, and close-out visits (onsite or remote) ensuring regulatory, ICH-GCP and GPP compliance.
• Verifies informed consent process and protects subject confidentiality; assesses safety and data integrity at investigator sites.
• Assesses site processes, conducts source document review, ensures CRF data quality, and drives timely query resolution.
• May manage IP inventory, storage, labeling, and release per protocol; ensures proper handling of blinded or randomized information.
• Maintains ISF accuracy and completeness; reconciles with TMF and supports archiving per guidelines.

Connaissances

Excellent communication

Presentation skills

Interpersonal skills

Good computer skills

Travel up to 75%

Formation

Bachelor’s degree or RN

Description du poste

Syneos Health, Inc. is recruiting a CRA I in Oncology based in the Paris area to monitor sites, ensure GCP compliance, and support trial execution for sponsor-dedicated projects. You will collaborate with cross-functional teams, manage site relationships, and travel up to 75% as required.

The role emphasizes regulatory knowledge, data integrity, and proactive site management to deliver high-quality trial results in a fast-paced environment.