Part-Time Clinical Research Coordinator — Poitiers

IQVIA LLC; Poitiers; Sur place; EUR 18 000 - 24 000; Temps partiel

Résumé du poste

IQVIA is seeking a Clinical Research Coordinator to support a clinical research site in Poitiers. This part-time role involves patient screening, consent handling, data entry, and documentation updates using CRFs and EDC systems.

The ideal candidate holds a life sciences degree, has 1–2 years of clinical research experience, and demonstrates strong communication, organizational, and IT skills in a regulated environment. Fluency in French and good English are required.

Qualifications

• Bachelor’s degree in life sciences or equivalent education and/or relevant experience in a clinical or medical setting.

Responsabilités

• Maintaining and updating study documentation, including protocols, CRFs, and EDC systems.
• Supporting patient screening and enrollment, including handling informed consent and privacy documentation.
• Coordinating logistical activities for study procedures in line with the study protocol.
• Performing data entry, quality checks, and resolving queries to ensure data accuracy and completeness.
• Patient education.
• Communicating with study monitors and responding to study-related inquiries.
• Carrying out general administrative tasks related to the study.

Connaissances

MS Office

French

English

Data entry

Interpersonal skills

Organizational skills

Clinical research

Formation

Bachelor’s degree in life sciences

Outils

MS Office

Description du poste

IQVIA is seeking a Clinical Research Coordinator to support a clinical research site in Poitiers. This part-time role involves patient screening, consent handling, data entry, and documentation updates using CRFs and EDC systems.

The ideal candidate holds a life sciences degree, has 1–2 years of clinical research experience, and demonstrates strong communication, organizational, and IT skills in a regulated environment. Fluency in French and good English are required.