At a Glance
- 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.
- Other info: This is a freelance role, offering approximately 0.25 FTE.
- 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.
The predicted salary is between 43200 - 72000 £ per year.
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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 in London employer: TFS HealthScience
As a forward-thinking global CRO, we pride ourselves on fostering a collaborative and innovative work culture that empowers our employees to make a meaningful impact in the lives of patients. Located in Luton, our hybrid model allows for flexibility while providing comprehensive benefits and ample opportunities for personal and professional growth, ensuring that you are supported every step of the way in your career journey.
StudySmarter Expert Advice🤫
We think this is how you could land Senior Clinical Research Associate in London
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Get involved with organisations such as the Royal Pharmaceutical Society or your local pharmaceutical professionals' network. Being an active member can boost your credibility and may even lead to job referrals in top organisations like TFS HealthScience.
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If you can, consider pursuing internships in the pharmaceutical industry, especially with companies like TFS HealthScience. These opportunities often pave the way for full-time positions and allow you to demonstrate your capabilities firsthand.
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We think you need these skills to ace Senior Clinical Research Associate in London
Some tips for your application 🫡
Showcase Your Relevant Experience:When applying for a role in the pharmaceutical industry, it's crucial to highlight any relevant experience you have. Whether that's internships, lab work, or even related coursework, make sure to weave this into your CV and cover letter. We want to see how your background aligns with the role you're applying for at TFS HealthScience!
Emphasise Your Understanding of Regulations:The pharmaceutical industry is heavily regulated, so it's important to indicate your familiarity with industry standards and regulations. In your cover letter, mention any training or certifications you've received that are relevant, or discuss projects where you’ve navigated compliance. This will show TFS HealthScience that you're not just a fit for the job but also a safety-conscious candidate!
Tailor Your CV to Be Result-Driven:Craft your CV to highlight quantifiable achievements, especially if you have previous roles in pharmaceuticals or related fields. Use metrics to demonstrate your impact, such as improved processing times or successful project completions while working on trials. This analytical approach will resonate well with hiring managers at TFS HealthScience!
Convey Your Passion for the Industry:In your cover letter, express why you are passionate about working in the pharmaceutical sector. Whether it’s your desire to contribute to groundbreaking drug research or improve patient outcomes, let it shine through! At TFS HealthScience, we value candidates who are truly enthusiastic about their work—you might just stand out from the crowd.
How to prepare for a job interview at TFS HealthScience
✨Understand the Science
Make sure you brush up on key pharmaceutical concepts and recent developments in the industry. You might get asked some technical questions during the interview at TFS HealthScience that show your grasp of drug development processes or regulatory requirements, so be ready to discuss them clearly.
✨Showcase Relevant Experience
If you have any hands-on experience or internships in a laboratory setting, be sure to highlight these in your responses. Think about the projects you worked on, the methodologies you used, and the impact you made. It's all about telling a story that connects your background to the role you're applying for.
✨Know Their Products
Take some time to familiarise yourself with TFS HealthScience’s product range and recent breakthroughs. Understanding their portfolio not only shows your enthusiasm for the role but also allows you to ask insightful questions that demonstrate your interest in actively contributing to their projects.
✨Be Ready for Regulatory Scenarios
In a full-time pharmaceutical role, understanding the regulatory landscape is crucial. Prepare for situational questions that may test your problem-solving skills concerning compliance and safety standards. You could be asked how you'd handle a hypothetical issue regarding a drug’s market release, so think through your approach.
