Part-Time Clinical Research Coordinator — Poitiers

IQVIA

Poitiers

Sur place

EUR 24 000 - 36 000

Temps partiel

14 jours+
Générateur de candidature

Une candidature sur mesure pour ce poste — un CV et une lettre de motivation personnalisés qui correspondent à l’offre.

Passez les filtres ATS

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

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.

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