Clinical Research Coordinator - Le Coudray

Location: Paris, France; onsite work at a clinical research site in Le Coudray

Company

hirify.global provides clinical research services, healthcare intelligence, and data-driven solutions for the life sciences and healthcare industries.

What you will do

• Maintain and update study documentation, including protocols, case report forms, and electronic data capture systems.
• Support patient screening and enrollment, including informed consent and privacy documentation.
• Coordinate logistics for study procedures in accordance with study protocols.
• Enter data, perform quality checks, and resolve queries to maintain data accuracy and completeness.
• Educate patients and communicate with study monitors regarding study-related inquiries.
• Complete general administrative tasks related to the clinical study.

Requirements

• Bachelor’s degree in life sciences or equivalent education and/or relevant clinical or medical experience.
• At least 1–2 years of experience as a Clinical Research Assistant, Research Nurse, or Clinical Research Coordinator at a clinical trial site.
• Understanding of clinical trials and familiarity with study protocols, consent forms, and schedules.
• Good knowledge of medical terminology and strong IT skills, including Outlook, Word, Excel, and Access.
• Strong interpersonal, communication, organizational, and attention-to-detail skills.
• Fluency in French and a good command of English.

Culture & Benefits

• Part-time schedule of 16 hours per week.
• Approximately six-month assignment.
• Supportive and collaborative research environment.
• Opportunity to contribute to clinical research advancing healthcare and patient outcomes.