Clinical Research Coordinator - Poitiers

IQVIA; Poitiers; Sur place; EUR 24 000 - 36 000; Temps partiel

Avantages offerts par ce poste

Restaurant d'entreprise

Indemnités de stage/alternance

Résumé du poste

IQVIA in Poitiers is seeking a part-time Clinical Research Coordinator (24 hours/week) to support a clinical research site. The role focuses on study documentation, patient screening, data entry, and study logistics in line with protocol.

The ideal candidate holds a life sciences bachelor’s degree, understands clinical trials, and has strong IT and communication skills in French and English. Immediate start for a ~6 month engagement.

Qualifications

• Bachelor's degree in life sciences or equivalent.
• Solid understanding of clinical trials and study protocols.
• Good knowledge of medical terminology.
• Strong IT skills with MS Office (Outlook, Word, Excel, Access).
• 1–2 years experience at a clinical trial site.
• Excellent interpersonal and communication skills.
• Fluency in French and good command of English.

Responsabilités

• Maintain and update study documentation (protocols, CRFs, EDC).
• Support patient screening and enrollment, including consent and privacy docs.
• Coordinate logistics for study procedures per protocol.
• Perform data entry and quality checks to ensure data accuracy.
• Educate patients about the study.
• Communicate with study monitors and respond to inquiries.
• Carry out general administrative tasks related to the study.

Connaissances

Interpersonal skills

Organizational skills

Attention to detail

Communication skills

French fluency

English proficiency

Formation

Bachelor's degree in Life Sciences

Outils

MS Office

Description du poste

Clinical Research Coordinator in Poitiers Working Hours: Part-time, 24h per week Start Date: Immediately Duration: Approximately 6 month IQVIA 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

• 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

• 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. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.