French-Speaking Field Clinical Research Associate – Travel‑Heavy in Selby

French-Speaking Field Clinical Research Associate – Travel‑Heavy in Selby

Selby Full-Time 40000 - 50000 £ / year (est.) No working from home possible
NAMSA

At a Glance

  • Tasks: Monitor clinical trials, ensuring compliance and subject protection across multiple sites.
  • Company: Join NAMSA, a leader in clinical research with a focus on innovation.
  • Benefits: Competitive salary, travel opportunities, and professional growth.
  • Other info: Enjoy a dynamic role with substantial travel and independence.
  • Why this job: Make a real difference in healthcare while exploring new places.
  • Qualifications: Fluent in English and French, with 3–5 years of monitoring experience.

The predicted salary is between 40000 - 50000 £ per year.

NAMSA is seeking a field-based Clinical Research Associate (CRA) to monitor trials and ensure GCP, regulatory compliance, and subject protection across multiple sites.

You will coordinate site visits, initiate and close study activities, and liaise with study teams to address enrollment and conduct issues.

Fluent English with French as a requirement, plus 3–5 years of monitoring experience.

The role involves substantial travel (8–9 visits per month across ~20 sites) and working independently

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French-Speaking Field Clinical Research Associate – Travel‑Heavy in Selby employer: NAMSA

NAMSA is an exceptional employer that values its employees by offering a dynamic work culture focused on professional growth and development. With extensive travel opportunities and the chance to work independently across diverse clinical sites, you will be part of a team dedicated to advancing medical research while enjoying a supportive environment that prioritises employee well-being and career progression.

NAMSA

Contact Details:

NAMSA Recruitment Team

We think you need these skills to ace French-Speaking Field Clinical Research Associate – Travel‑Heavy in Selby

Fluent English
Fluent French
Clinical Research Monitoring
GCP Compliance
Regulatory Compliance
Subject Protection
Site Coordination