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

## Clinical Research Coordinator - PoitiersApplylocations: Poitiers, Francetime type: Part timeposted on: Posted Todayjob requisition id: R1558813**Clinical Research Coordinator in Poitiers****Working Hours:** Part-time, 24h per week **Start Date**: Immediately **Duration**: Approximately 6 monthIQVIA is currently recruiting a dedicated Clinical Research Coordinator to support a clinical research site in Poitiers. This part-time position offers a unique opportunity to contribute to meaningful research in a collaborative and dynamic environment.**Key Responsibilities** As a vital member of the site team, you will help ensure the smooth execution of the clinical trial by performing a range of administrative and clinical support tasks, including:* Maintaining and updating study documentation, including protocols, case report forms (CRFs), and Electronic Data Capture (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**Your Profile** We are looking for candidates who bring a combination of education, experience, and skills:* Bachelor’s degree in life sciences or equivalent education and/or relevant experience in a clinical or medical setting (e.g., clinical research coordinator, research assistant, nurse, medical assistant)* Solid understanding of clinical trials and familiarity with study protocols, consent forms, and schedules* good knowledge of medical terminology* Strong IT skills, including proficiency in MS Office applications (Outlook, Word, Excel, Access)* **Must have at least 1-2 years experience working as a Clinical Research Assistant, Research Nurse or Clinical Research Coordinator at a clinical trial site*** Excellent interpersonal and communication skills* Strong organizational skills and attention to detail* Fluency in French and good command of English**Why Join IQVIA?** At IQVIA, you will be part of a global team that is advancing healthcare through data, technology, and human science. We offer a supportive work environment, impactful projects, and the opportunity to make a real difference.**Interested?** If this sounds like the right opportunity for you, we encourage you to apply today.