Clinical Data Officer — Medical Affairs & Trials

Excelya; France; Remote; EUR 45,000 - 60,000; Full time

Job summary

Excelya seeks a Medical Data Officer to join our Medical Affairs team in France. You will collaborate with the Study Medical Reviewer to ensure medical data accuracy and analyzability across the database. The role emphasizes safety data coding, data validation, and rigorous medical review.

The ideal candidate has 12 months in clinical trials or therapeutic development, strong communication skills, and a medical or scientific background (MD, pharmacist, or scientist). English fluency is required.

Qualifications

• Experience in clinical trials and therapeutic development is preferred, with at least 12 months in the field.
• Strong interpersonal and communication skills with well organized prioritization.
• Languages: Fluency in English; ability to work in a cross-functional team.

Responsibilities

• Review protocols with focus on safety management and data coding criteria.
• Review database specifications and perform UAT on eCRF and validation tools.
• Identify protocol deviations and implement detection methods as required.
• Code adverse events and medical history; review study data with investigators.
• Identify non-serious AEs and support data extraction for milestones.

Skills

Clinical trials

Medical data review

Communication skills

Organization

Education

Medical Doctor / Pharmacist / Scientist

Job description

Excelya seeks a Medical Data Officer to join our Medical Affairs team in France. You will collaborate with the Study Medical Reviewer to ensure medical data accuracy and analyzability across the database. The role emphasizes safety data coding, data validation, and rigorous medical review.

The ideal candidate has 12 months in clinical trials or therapeutic development, strong communication skills, and a medical or scientific background (MD, pharmacist, or scientist). English fluency is required.