At a Glance
- Tasks: Manage clinical trials, ensuring patient safety and data quality while building strong site relationships.
- Company: TFS HealthScience, a leading global Contract Research Organization dedicated to clinical development.
- Benefits: Opportunities for personal growth, collaborative culture, and making a real difference in patients' lives.
- Other info: Dynamic environment with a focus on trust, quality, and sustainability.
- Why this job: Join a passionate team and contribute to groundbreaking oncology research that impacts patient care.
- Qualifications: Bachelor's 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. 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.
- 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.
- 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.
- 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. 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 (CRA) - Oncology in London employer: Trial Form Support
TFS HealthScience is an exceptional employer, offering a dynamic work environment where innovation and collaboration thrive. As a Senior Clinical Research Associate, you will benefit from a competitive compensation package and comprehensive benefits, while also having the opportunity for personal and professional growth in a rewarding setting. With a strong emphasis on core values such as Trust, Quality, and Sustainability, TFS fosters a culture of mutual respect and engagement, making it a fulfilling place to advance your career in clinical research.
