Senior Clinical Quality Manager

TFS HealthScience; London; Hybrid; GBP 50,000 - 75,000; Full time

Job summary

TFS HealthScience, a prominent global mid-size CRO, seeks a Quality Manager to uphold clinical study standards. The role involves ensuring compliance with regulations, training staff, and is based in London with hybrid flexibility. Join a team dedicated to making a difference in patients' lives through innovative research.

Benefits

Competitive compensation package

Comprehensive benefits

Opportunities for personal and professional growth

Qualifications

• Minimum 5 years of experience in the pharmaceutical industry.
• Good knowledge of ICH-GCP and study management.
• Ability to multitask and complete objectives efficiently.

Responsibilities

• Provide advice on local regulations and ensure compliance.
• Support operational staff in audits and inspections.
• Prepare and deliver training as appropriate.

Skills

Communication

Planning

Problem Solving

Organizational

Education

Bachelor's 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) partnering with biotechnology and pharmaceutical companies throughout their clinical development journey. Our expertise includes full-service capabilities, resourcing, and Functional Service Provider (FSP) solutions.

The Quality Manager is responsible for maintaining, developing, and communicating high-quality standards in the delivery of clinical studies.

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

Key Responsibilities:

• Provide competent advice on local regulations related to clinical trials, stay updated on changes, and ensure local teams and processes are compliant.
• Support and guide operational staff in preparing for audits and inspections, including risk analysis and developing inspection readiness strategies.
• Prepare and deliver training as appropriate.
• Participate in internal meetings and liaise with other departments as necessary.
• Maintain knowledge of applicable regulations, standards, and procedures.

Qualifications:

• Bachelor's degree in a related discipline.
• Minimum of 5 years of experience in the pharmaceutical industry, preferably in Clinical Operations or Quality Assurance.
• Good knowledge of ICH-GCP, study management, site management, and monitoring.
• Excellent communication skills.
• Strong planning, organizational, and problem-solving abilities.
• Proficient in MS Office applications.
• Ability to multitask, prioritize, and complete objectives efficiently.

What We Offer

We offer a competitive compensation package, comprehensive benefits, and opportunities for personal and professional growth in a rewarding environment. Join a team that values collaboration, innovation, and making a difference in patients' lives.

A Bit More About Us

Founded over 27 years ago in Lund, Sweden, TFS HealthScience is a full-service, global CRO with over 800 professionals. We deliver tailored clinical research services in more than 40 countries, focusing on therapeutic areas including Dermatology, Neuroscience, Oncology, and Ophthalmology.

Our core values—Trust, Quality, Passion, Flexibility, and Sustainability—guide our decision-making and culture. We aim to attract and retain talented individuals who share these values, fostering high engagement and collaboration. Together we make a difference.

Department: SRS Mid Europe

Location: London (Hybrid)

Employment Type: Full-time

REQ ID: reqID277162