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Senior Clinical Quality Manager

TFS HealthScience

London

Hybrid

GBP 40,000 - 80,000

Full time

30+ days ago

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Job summary

An established industry player is seeking a Quality Manager to uphold high standards in clinical studies. This hybrid role offers the chance to work closely with biotech and pharmaceutical companies, ensuring compliance with local regulations and fostering a culture of quality. You'll be part of a collaborative team dedicated to making a significant impact on patient lives. With over 27 years of experience, this forward-thinking organization values innovation and personal growth, providing a competitive compensation package and comprehensive benefits. Join a mission-driven environment where your expertise will be essential in shaping the future of clinical research.

Qualifications

  • 5+ years in the pharmaceutical industry, focusing on Clinical Operations/Quality Assurance.
  • Strong knowledge of ICH-GCP and study management.

Responsibilities

  • Advise on local regulations for clinical trials and keep teams updated.
  • Support operational staff in audit preparation and inspection readiness.

Skills

Communication Skills
Planning
Problem-Solving
Multitasking

Education

Bachelor degree in a related discipline

Tools

MS Office

Job description

About this role

TFS HealthScience is a leading global mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire clinical development journey. Our expertise includes full service capabilities, resourcing and Functional Service (FSP) solutions.

The Quality Manager is responsible for the maintenance and further development, and the communication of high-quality standards in the delivery of clinical studies.

This is a hybrid role, with 3 days on-site.

Key Responsibilities:

  1. Provides competent advice on local regulations related to clinical trials, keeps abreast of changes in local regulations related to clinical trials and keeps local teams and local processes updated.
  2. Assist with supporting and guiding operational staff in preparing for audits and inspections including analysing risks and developing inspection readiness strategy.
  3. Prepares and presents training as appropriate.
  4. Participate in internal meetings as required and liaise with other departments as necessary.
  5. Maintain required knowledge of applicable regulations and company standards and procedures.

Qualifications:

  1. Bachelor degree in a related discipline.
  2. At least 5 years of experience in the pharmaceutical industry, preferably in Clinical Operations/Quality Assurance.
  3. Good knowledge and understanding of ICH-GCP, study management, site management, monitoring.
  4. Excellent communication skills.
  5. Good planning, organisation and problem-solving abilities.
  6. Advanced user of MS Office applications.
  7. Demonstrated ability to multitask, prioritize, and complete objectives.

What We Offer

We provide a competitive compensation package, comprehensive benefits, and the opportunity for personal and professional growth in a rewarding environment. You'll be joining a team that values collaboration, innovation, and making a difference in the lives of patients.

A Bit More About Us

Our journey began over 27 years ago in Sweden, in the city of Lund. As a full-service, global Contract Research Organization (CRO), we build solution-driven teams working towards a healthier future. Bringing together over 800 professionals, TFS delivers tailored clinical research services in more than 40 countries with flexible clinical development and strategic resourcing solutions across key therapeutic areas including Dermatology, Neuroscience, Oncology, and Ophthalmology.

Our core values of Trust, Quality, Passion, Flexibility, and Sustainability are our guiding light serving as the framework for decision-making at all levels of the organization. They assist us in attracting and retaining valuable talent who share our sentiments, resulting in high employee engagement and satisfaction. By aligning on these fundamental values, we cultivate a unified force, geared towards innovation and excellence. This collective effort propels us towards our shared goal and fosters a culture of mutual respect and collaboration. Together we make a difference.

Department: SRS Mid Europe

Locations: London

Remote status: Hybrid

Employment type: Full-time

REQ ID: reqID277162

Work Arrangement: Hybrid

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