Global QA Project Manager - Oncology (GCP/GMP), Hybrid

Global QA Project Manager - Oncology (GCP/GMP), Hybrid

Full-Time 60000 - 80000 Β£ / year (est.) No working from home possible
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At a Glance

  • Tasks: Lead QA activities in global clinical trials and ensure compliance with regulatory requirements.
  • Company: Ellipses Pharma, a dynamic player in the pharmaceutical sector.
  • Benefits: Hybrid work environment, competitive salary, and opportunities for professional growth.
  • Other info: Join a supportive team focused on innovation and quality.
  • Why this job: Make a real impact in oncology while ensuring high-quality standards in clinical trials.
  • Qualifications: Minimum five years in the pharmaceutical sector with GCP expertise.

The predicted salary is between 60000 - 80000 Β£ per year.

Ellipses Pharma in the City of Westminster is seeking a Quality Assurance Project Manager to lead QA activities in global clinical trials. The candidate will ensure compliance with regulatory requirements while overseeing quality systems.

With at least five years in the pharmaceutical sector and expertise in operational GCP, this role entails creating audit programmes and maintaining quality standards. A hybrid work environment is supported.

Global QA Project Manager - Oncology (GCP/GMP), Hybrid employer: Ellipses Pharma

Ellipses Pharma is an exceptional employer that fosters a collaborative and inclusive work culture, where face-to-face interaction is highly valued. With a strong focus on employee growth and development, the company offers opportunities to engage with leading Oncology experts while supporting a hybrid work model that promotes work-life integration. Joining Ellipses means being part of a dynamic team dedicated to advancing innovative oncology treatments in a supportive environment.

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Contact Details:

Ellipses Pharma Recruitment Team

We think you need these skills to ace Global QA Project Manager - Oncology (GCP/GMP), Hybrid

Quality Assurance
GCP (Good Clinical Practice)
GMP (Good Manufacturing Practice)
Regulatory Compliance
Audit Programme Development
Quality Systems Management
Pharmaceutical Industry Experience