Freelance Clinical Research Coordinator - Lille (France)

Proclinical Staffing; Lille; Sur place; EUR 40 000 - 60 000; Temps partiel

Résumé du poste

A leading life sciences recruitment agency is seeking a Freelance Clinical Research Coordinator in Lille. The role involves supporting clinical research activities, ensuring data accuracy, and managing administrative tasks on a part-time basis. Candidates should have relevant experience and proficiency in both French and English. This freelance opportunity offers flexible working hours, requiring availability for one day per week with an immediate start and potential contract renewal.

Qualifications

• Previous experience as a Study Coordinator, Clinical Research Coordinator, or similar role.
• Strong organisational skills and attention to details.
• Ability to work independently and manage tasks efficiently.
• Proficiency in both French and English.

Responsabilités

• Perform data entry and ensure data accuracy.
• Manage query resolution in a timely manner.
• Handle administrative tasks and maintain study documentation.
• Upload and organise study images and related files.
• Support the day-to-day coordination and follow-up of study activities.

Connaissances

Organisational skills

Attention to detail

Ability to work independently

Proficiency in French

Proficiency in English

Description du poste

Drive clinical research forward-join us as a Freelance Clinical Research Coordinator in Lille and make an impact one study at a time!

Freelance Senior Clinical Research Coordinator (ARC TEC) - Lille

Location: Lille, France
Contract: Freelance / Independent contractor
Duration: 3 months, renewable
Workload: 1 day per week
Start date: Immediate

Proclinical is seeking a Freelance Clinical Research Coordinator based in Lille, France. In this role, you will support clinical research activities, focusing on data entry, query resolution, and administrative tasks. This is a part-time, freelance opportunity requiring availability for one day per week, with an immediate start and potential for contract renewal.

Key Responsibilities

• Perform data entry and ensure data accuracy.
• Manage query resolution in a timely manner.
• Handle administrative tasks and maintain study documentation.
• Upload and organise study images and related files.
• Support the day-to-day coordination and follow-up of study activities.

Profile

• Previous experience as a Study Coordinator, Clinical Research Coordinator, or similar role.
• Strong organisational skills and attention to details.
• Ability to work independently and manage tasks efficiently.
• Proficiency in French and English.
• Availability 1 day per week, based in or near Lille

If you are having difficulty in applying or if you have any questions, please contact Camille Sandres at [e-mail].

Apply Now

If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists please request a call back at the top of this page.

Proclinical is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Proclinical is acting as an Employment Agency in relation to this vacancy.

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