Remote GCP Auditor & QA Compliance Lead

Remote GCP Auditor & QA Compliance Lead

Full-Time 50000 - 70000 Β£ / year (est.) No working from home possible
Precision Medicine Group

At a Glance

  • Tasks: Conduct audits and provide QA guidance for global trials in a fully remote role.
  • Company: Join Precision for Medicine, a leader in quality management in clinical trials.
  • Benefits: Enjoy a competitive salary, flexible work environment, and opportunities for travel.
  • Other info: Dynamic role with opportunities for professional growth and international travel.
  • Why this job: Make a real impact on global health by ensuring compliance in innovative trials.
  • Qualifications: Experience in GCP auditing and knowledge of FDA and ICH guidelines required.

The predicted salary is between 50000 - 70000 Β£ per year.

Precision for Medicine seeks a full-time GCP Auditor for a fully remote role.

You will support the Quality Management System, conduct audits, and provide QA guidance across global trials.

Travel up to 25% domestically and internationally is required.

Responsibilities include coordinating vendor and site audits, training staff, and maintaining CAPA processes in line with US FDA, EU ICH, and company policies.

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Remote GCP Auditor & QA Compliance Lead employer: Precision Medicine Group

At Precision Medicine Group, we pride ourselves on being an excellent employer by fostering a collaborative and innovative work culture that empowers our employees to make a real impact in the field of clinical research. With fully remote opportunities across the UK, we offer flexible working arrangements, comprehensive benefits, and continuous professional development to support your career growth. Join us to be part of a team that values your contributions and is dedicated to advancing healthcare outcomes.

Precision Medicine Group

Contact Details:

Precision Medicine Group Recruitment Team

We think you need these skills to ace Remote GCP Auditor & QA Compliance Lead

GCP Auditing
Quality Management System
Audit Coordination
CAPA Processes
US FDA Regulations
EU ICH Guidelines
Training and Development