Clinical Research Nurse

Meet Life Sciences; Montpellier; Sur place; EUR 22 320 - 33 480; Temps partiel

Résumé du poste

A leading company in clinical research is seeking a Customer Success Partner focusing on dermatological studies. The role is contract-based, requiring approximately 20 hours a month, and involves hands-on clinical responsibilities like patient recruitment and data management. Ideal candidates will have clinical experience, particularly in wound care, and preferred certifications in GCP and life support. This part-time position allows for both center-based and homecare responsibilities.

Qualifications

• Minimum of two years’ experience in a study nurse or similar clinical role.
• Prefer certifications in GCP, IATA, and Basic Life Support.

Responsabilités

• Support patient recruitment through site visits.
• Conduct home visits as needed for patient care.
• Ensure accuracy of patient data in study protocols.

Connaissances

Clinical expertise

Wound care

Patient care

Data accuracy

Formation

Clinical qualifications

Description du poste

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Customer Success Partner @ Meet Life Sciences

Commitment: Approximately 20 hours per month

Duration: 18–24 months

Area of Focus: Dermatological studies

Candidate Profile:

We are seeking a qualified clinical professional with:

• A minimum of two years’ hands-on experience in a study nurse or similar clinical role
• Specific expertise in wound care
• Preferred certifications: GCP, IATA, and Basic Life Support

Project Scope:

The role involves contributing to a long-term clinical study through a combination of centre-based and homecare responsibilities, including:

• Supporting patient recruitment efforts through site visits
• Conducting occasional home visits as needed
• Managing and maintaining pre-screening documentation
• Assisting in the development of study-specific worksheets where relevant
• Providing patient care in alignment with study protocols and guidelines
• Accurately recording patient data per protocol requirements
• Ensuring the accuracy and quality of data entries in source documents and electronic CRFs, in close collaboration with the study team and physicians
• Reviewing key study documentation such as informed consent forms and safety reports
• Coordinating communication with study sites, sponsors, CROs, and internal teams
• Being accessible for appointment scheduling with study centres

Seniority level

• Seniority level

  Mid-Senior level

Employment type

• Employment type

  Contract

Job function

• Job function

  Health Care Provider

• Industries

  Hospitals and Health Care

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