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- Tasks: Lead site monitoring for ophthalmology trials and ensure compliance with protocols.
- Company: TFS HealthScience is a global CRO focused on innovative therapies in clinical research.
- Benefits: Enjoy flexible remote work and the chance to contribute to groundbreaking studies.
- Why this job: Join a passionate team dedicated to improving patient outcomes in ophthalmology.
- Qualifications: Experience in clinical trial monitoring and ophthalmology, especially retinal disorders.
- Other info: This is a freelance role, offering approximately 0.25 FTE.
The predicted salary is between 43200 - 72000 ÂŁ per year.
Join to apply for the Senior Clinical Research Associate role at TFS HealthScience
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Join to apply for the Senior Clinical Research Associate role at TFS HealthScience
TFS HealthScience is a global, mid-sized Contract Research Organization (CRO) dedicated to supporting biotechnology and pharmaceutical companies throughout their clinical development journey. We provide full-service capabilities, resourcing, and Functional Service Provider (FSP) solutions to help bring innovative therapies to patients worldwide.
We are currently seeking a Senior Clinical Research Associate (SCRA) based in the United Kingdom, with strong oncology experience and a proven track record in clinical trial monitoring. In this role, you will support a key sponsor in delivering high-quality oncology studies, ensuring regulatory compliance and excellent site performance throughout the trial lifecycle.
TFS HealthScience is a global, mid-sized Contract Research Organization (CRO) dedicated to supporting biotechnology and pharmaceutical companies throughout their clinical development journey. We provide full-service capabilities, resourcing, and Functional Service Provider (FSP) solutions to help bring innovative therapies to patients worldwide.
We are currently seeking a Senior Clinical Research Associate (SCRA) based in the United Kingdom, with strong oncology experience and a proven track record in clinical trial monitoring. In this role, you will support a key sponsor in delivering high-quality oncology studies, ensuring regulatory compliance and excellent site performance throughout the trial lifecycle.
Key Responsibilities
Independently manage all aspects of site monitoring for oncology trials, including pre-study, initiation, routine, and close-out visits
Ensure trial conduct aligns with protocols, ICH-GCP, and applicable local/international regulatory requirements
Act as the main point of contact for investigative sites, building strong site relationships to support trial success
Monitor patient safety, data integrity, and compliance through regular site visits and risk-based monitoring strategies
Participate in ethics and regulatory submissions, site activation, and investigator training as needed
Support cross-functional project teams in meeting timelines and quality standards
Qualifications
Minimum 3–5 years of independent site monitoring experience within CRO, biotech, or pharmaceutical environments
Oncology therapeutic experience and CAR-T experienceis required
Strong understanding of ICH-GCP and applicable UK regulatory requirements
Proven ability to manage multiple sites and trials independently
Excellent communication and interpersonal skills
Ability to travel for on-site visits as required
A Bit More About Us
Founded over 27 years ago in Lund, Sweden, TFS HealthScience is a full-service, global CRO with more than 800 professionals delivering tailored clinical research services in over 40 countries. We offer flexible clinical development and strategic resourcing solutions across key therapeutic areas, including Oncology, Neuroscience, Dermatology, and Ophthalmology.
Our core values—Trust, Quality, Passion, Flexibility, and Sustainability—guide our decisions and define our culture. They help us attract and retain exceptional talent, fostering a high level of engagement, collaboration, and mutual respect. Together, we drive innovation and make a meaningful impact in the world of clinical research.
Seniority level
-
Seniority level
Not Applicable
Employment type
-
Employment type
Full-time
Job function
-
Job function
Research, Analyst, and Information Technology
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Industries
Pharmaceutical Manufacturing
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Senior Clinical Research Associate employer: TFS HealthScience
Contact Detail:
TFS HealthScience Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Senior Clinical Research Associate
✨Tip Number 1
Network with professionals in the ophthalmology field, especially those who have experience in clinical trials. Attend relevant conferences or webinars to connect with potential colleagues and learn about the latest trends in retinal disorders.
✨Tip Number 2
Familiarise yourself with the specific regulatory requirements for clinical trials in the UK, particularly those related to ophthalmology. This knowledge will not only boost your confidence but also demonstrate your commitment to compliance during interviews.
✨Tip Number 3
Prepare to discuss your previous experiences in clinical trial monitoring, focusing on any challenges you faced and how you overcame them. Highlighting your problem-solving skills will show that you're ready for the proactive issue resolution required in this role.
✨Tip Number 4
Research TFS HealthScience's recent projects and publications in gene therapy and retinal diseases. Being knowledgeable about their work will help you engage in meaningful conversations during interviews and show your genuine interest in joining their team.
We think you need these skills to ace Senior Clinical Research Associate
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your relevant experience in clinical trial monitoring, particularly in ophthalmology and retinal disorders. Use specific examples to demonstrate your expertise and achievements in these areas.
Craft a Compelling Cover Letter: Write a cover letter that not only outlines your qualifications but also expresses your passion for clinical research and the specific role at TFS HealthScience. Mention your familiarity with gene therapy and how it aligns with their projects.
Highlight Regulatory Knowledge: Emphasise your understanding of local and international regulatory requirements in your application. This is crucial for the role, so provide examples of how you've ensured compliance in past projects.
Showcase Interpersonal Skills: Since the role involves engaging with sponsors and site staff, include examples in your application that demonstrate your strong interpersonal skills and ability to work collaboratively in a team environment.
How to prepare for a job interview at TFS HealthScience
✨Showcase Your Ophthalmology Expertise
Make sure to highlight your experience in ophthalmology, especially with retinal disorders. Be prepared to discuss specific trials you've worked on and how your contributions led to successful outcomes.
✨Understand Regulatory Requirements
Familiarise yourself with both local and international regulatory requirements relevant to clinical trials. Demonstrating your knowledge in this area will show that you can ensure compliance and maintain high-quality standards.
✨Emphasise Risk-Based Monitoring Skills
Discuss your approach to risk-based monitoring and how you've implemented proactive issue resolution in past roles. Providing examples of how you've maintained trial quality through these methods will be beneficial.
✨Engage Effectively with Stakeholders
Prepare to talk about your interpersonal skills and how you've successfully engaged with sponsors and site staff. Highlighting your ability to build strong relationships will demonstrate your fit for the collaborative culture at TFS HealthScience.
