Clinical Quality Manager

HRM - Delivering Leadership Talent

England

On-site

GBP 36,000 - 42,000

Full time

14 days+

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Job summary

A leading healthcare solutions provider in the UK is seeking a Clinical Quality Manager to oversee clinical quality management systems. This role requires strong leadership and collaboration with cross-functional teams to ensure compliance with regulatory standards. Candidates should have over 5 years of experience in clinical quality oversight and a Bachelor’s degree in a relevant field.

Qualifications

  • 5+ years' experience in a Clinical Quality oversight role.
  • Experience in audits and/or quality oversight processes in GxP areas.
  • Experience carrying out regulatory inspections.

Responsibilities

  • Develop and maintain an effective clinical quality management system.
  • Collaborate with cross-functional teams to support clinical trial programs.
  • Ensure GCP/ICH-compliant systems are established and maintained.

Skills

Clinical QA experience
Strong communication skills
Presentation skills

Education

Bachelor's Degree in Science

Job description

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HRM - Delivering Leadership Talent provided pay range

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Base pay range

For over a century and five generations, this family-owned company has been dedicated to improving lives through innovative healthcare solutions, particularly in hormonal treatments for women's and men's health.

Now seeking a Clinical Quality Manager (GCP), the company continues to build on its legacy of pioneering breakthroughs. Over the past 20 years, they have expanded into a global operation with a direct presence in 22 countries and a multicultural team of 1,500 employees worldwide - having doubled in size in recent years. Generating $500 million in annual revenues, their remarkable growth is driven by a commitment to innovation, diversity, and a deep understanding of what truly matters to patients and their families.

The Position

  • Develop and maintain an effective clinical quality management system to oversee investigational sites and vendors.
  • Collaborate with cross-functional teams (Clinical Operations, Project Management Office, Medical, Regulatory, Pharmacovigilance, etc.) to support clinical trial programs for both new products and new indications of marketed products.
  • Ensure GCP/ICH-compliant systems and processes are established and maintained to uphold the quality of clinical trials conducted globally and locally, as needed.
  • Contribute to the development, review, and continuous improvement of clinical processes and Standard Operating Procedures (SOPs).
  • Monitor adherence to applicable SOPs, guidelines, and regulatory requirements across clinical activities.
  • Oversee inspection readiness efforts, including planning and coordination of inspection-related activities.
  • Assess and qualify Clinical Research Organizations (CROs) and other vendors involved in clinical operations.
  • Develop audit plans, and conduct investigator site audits to ensure compliance with protocols, Good Clinical Practice (GCP), and applicable regulations.
  • Oversee CRO and investigator monitoring activities to ensure alignment with protocols, GCP, regulatory requirements, and internal policies.
  • Manage quality records, including change controls, investigations, deviations, and Corrective and Preventive Actions (CAPAs), ensuring timely resolution and closure.

The Person

  • Bachelor's Degree (Science discipline preferred).
  • 5+ years' experience in a Clinical Quality oversight role.
  • Clinical QA experience in the pharmaceutical industry essential.
  • Experience in audits and/or quality oversight processes in GxP areas.
  • Experience carrying out regulatory inspections.
  • You work independently as well as collaboratively with cross functional teams.
  • Strong communication skills both written and verbal.
  • Excellent presentation and training skills.

To learn more about this role apply online or contact Anita Osibuamhe on +44 (20) 3769 7178 for a confidential discussion.

Seniority level
  • Seniority level
    Mid-Senior level
Employment type
  • Employment type
    Full-time
Job function
  • Job function
    Quality Assurance
  • Industries
    Pharmaceutical Manufacturing

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