At a Glance
- Tasks: Support clinical trials by ensuring patient safety and data quality while managing site activities.
- Company: Join TFS HealthScience, a leading global Contract Research Organization dedicated to improving patient lives.
- Benefits: Enjoy personal and professional growth in a collaborative environment with a focus on quality and innovation.
- Other info: Be part of a diverse team committed to excellence across over 50 countries.
- Why this job: Make a real difference in healthcare by working closely with industry leaders in clinical research.
- Qualifications: Bachelor's degree in Life Sciences and 3-4 years of CRA experience preferred.
The predicted salary is between 40500 - 49500 £ per year.
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.
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.
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.
Clinical Research Associate in England employer: TFS HealthScience
TFS HealthScience is an exceptional employer, offering a dynamic and supportive work environment that prioritises collaboration and innovation. With a strong commitment to employee growth, we provide comprehensive benefits and opportunities for professional development, ensuring that our team members can thrive in their careers while making a meaningful impact in the clinical research field. Join us in our mission to improve patient lives, where your contributions are valued and recognised within a culture built on trust and excellence.
