Onsite Oncology CRC — Medidata Rave Expert

RapidTrials; Marseille; Sur place; EUR 83 000 - 117 000; Plein temps

Résumé du poste

RapidTrials seeks an onsite coordination and data support for an industry-sponsored study of an investigational medicine for advanced, metastatic or recurrent head and neck squamous cell carcinoma. The role focuses on accurate study data, timely query resolution and well-maintained site documentation.

The contract is for about 8 hours per week over 12 weeks, onsite in Marseille, France, and performed as independent professional services via a French auto-entreprise.

Qualifications

• At least 2 years of clinical research coordination or relevant research nursing experience (oncology preferred).
• Hands-on Medidata Rave experience with data entry and query resolution.
• IST-GCP training and knowledge of European trial requirements and ethics.
• Fluent written and spoken French and English; strong organisation and attention to detail.
• Bachelor's degree or equivalent preferred; suitable clinical research experience may substitute.
• Evidence of business registration and eligibility to practice independently in France (auto-entreprise/SIREN/SIRET).

Responsabilités

• Enter and reconcile study data in Medidata Rave and other approved EDC systems within timelines.
• Resolve data queries and refer clinical questions to the investigator.
• Prepare and maintain the investigator site file, training and delegation records, study logs and consent documents.
• Support submissions to CPP and ANSM and help coordinate monitoring visits.
• Join study calls and assist with close out of documented follow-up actions.
• Coordinate participant travel reimbursements and visit logistics.
• Promptly escalate potential adverse events and safety concerns as required.

Connaissances

Medidata Rave

French & English

Microsoft Office

Data coordination

On-site coordination

Formation

Bachelor's degree or equivalent

Outils

Medidata Rave

Microsoft Office

Description du poste

RapidTrials seeks an onsite coordination and data support for an industry-sponsored study of an investigational medicine for advanced, metastatic or recurrent head and neck squamous cell carcinoma. The role focuses on accurate study data, timely query resolution and well-maintained site documentation.

The contract is for about 8 hours per week over 12 weeks, onsite in Marseille, France, and performed as independent professional services via a French auto-entreprise.