Clinical Research Associate

TFS; City of Westminster; On-site; GBP 35,000 - 55,000; Full time

Job summary

TFS HealthScience is seeking a Clinical Research Associate (CRA) to support delivery of clinical trials across designated sites in the United Kingdom. You will ensure patient safety, data quality, protocol compliance and strong site performance while taking ownership of site management activities.

As part of our global mid-size CRO, you will build effective relationships with investigators and site staff, document and resolve issues, and collaborate with project teams to achieve study

Qualifications

• Bachelor's degree in Life Sciences or related field.
• 3-4 years of Clinical Research Associate experience in pharma/biotech/CRO.
• Strong organizational, communication and stakeholder management skills.
• Oncology and/or Phase I experience is preferred but not essential.

Responsibilities

• Conduct site qualification, initiation, monitoring and close-out visits per protocol, ICH-GCP and regulations.
• Ensure subject safety, data integrity and protocol compliance throughout the study lifecycle.
• Build and maintain relationships with investigators, study coordinators and site staff.
• Identify, document and proactively resolve site issues, risks and recruitment challenges.
• Complete monitoring reports and maintain study documentation and trial systems.
• Collaborate with project teams to ensure study milestones and deliverables are met.

Skills

Organizational skills

Communication skills

Stakeholder management

Education

Bachelor's degree in Life Sciences or related field

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.

We are seeking a Clinical Research Associate (CRA) to support the successful delivery of clinical trials across designated sites. In this role, you will be responsible for ensuring patient safety, data quality, protocol compliance, and strong site performance while taking ownership of site management activities and building effective relationships with investigators and site staff.

As part of our Functional Solutions team, you will be dedicated to one sponsor, a global pharmaceutical company that is an industry leader within its therapeutic area.

Key Responsibilities

• Conduct site qualification, initiation, monitoring, and close-out visits in accordance with study protocols, ICH-GCP, and applicable regulations
• Ensure subject safety, data integrity, and protocol compliance throughout the study lifecycle
• Build and maintain strong relationships with investigators, study coordinators, and site personnel
• Identify, document, and proactively resolve site issues, risks, and recruitment challenges
• Complete monitoring reports and maintain accurate study documentation and trial management systems
• Collaborate with project teams and stakeholders to ensure study milestones and deliverables are achieved

Qualifications

• Bachelor's degree in Life Sciences or a related field
• 3-4 years of Clinical Research Associate experience within the pharmaceutical, biotechnology, or CRO industry
• Strong organizational, communication, and stakeholder management skills
• Demonstrated ability to work independently and take ownership of site activities and deliverables
• Solid understanding of ICH-GCP, clinical trial processes, and applicable regulations
• Oncology and/or Phase I clinical trial experience is preferred but not essential

What We Offer

We provide opportunities for personal and professional growth in a rewarding environment. You will join a team that values collaboration, quality, and making a difference in the lives of patients.

Our core values of Trust, Quality, Passion, Flexibility, and Sustainability guide our decisions and shape our culture. By aligning on these values, we foster collaboration, innovation, and a shared commitment to excellence. Together, we make a difference.

A Bit More About Us

Our journey began over 30 years ago in Sweden, in the city of Lund. As a full-service global CRO, we build solution-driven teams working toward a healthier future. Bringing together over 600 professionals, TFS delivers tailored clinical research services in more than 50 countries, offering flexible clinical development and strategic resourcing solutions across key therapeutic areas including Dermatology, Neuroscience, Oncology, and Ophthalmology.