Find a job 
Featured Companies 
Featured Universities 
For Companies At a Glance
- Tasks: Lead site monitoring for ophthalmology trials, ensuring quality and compliance.
- Company: Global CRO dedicated to innovative clinical research in healthcare.
- Benefits: Flexible freelance role with a focus on professional growth and impactful work.
- Why this job: Join a passionate team driving cutting-edge research that makes a real difference.
- Qualifications: Experience in clinical trial monitoring and strong ophthalmology knowledge required.
- Other info: Collaborative culture with a commitment to trust, quality, and sustainability.
The predicted salary is between 40000 - 50000 £ per year.
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 (0.45 FTE) with strong ophthalmology experience. This role involves working with a key sponsor on ophthalmology studies, ensuring high quality study execution, regulatory compliance, and effective site management across the full monitoring lifecycle. This is a long term freelance assignment at 0.45 FTE.
Key Responsibilities:- Lead site monitoring activities for ophthalmology trials, ensuring adherence to protocol, GCP, and regulatory requirements.
- Implement risk-based approaches to ensure proactive issue resolution and maintain trial quality.
- Manage ethics committee submissions, amendments, and periodic regulatory reporting, including safety event notifications.
- Contribute to site activation, including Site Initiation Visits (SIVs) and investigator training.
- Ensure proper trial documentation, monitor data integrity, and support study closeout.
- Prior experience in clinical trial monitoring within a CRO, biotech, or pharmaceutical company.
- At least 1 year of therapeutic expertise in ophthalmology trials.
- Familiarity with local and international regulatory requirements.
- Strong interpersonal skills to engage effectively with sponsors and site staff.
Join us in driving forward cutting-edge clinical research in ophthalmology and beyond.
Senior Clinical Research Associate in City of Westminster employer: TFS HealthScience
Contact Detail:
TFS HealthScience Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Senior Clinical Research Associate in City of Westminster
✨Tip Number 1
Network like a pro! Reach out to your connections in the clinical research field, especially those with experience in ophthalmology. A friendly chat can lead to insider info about job openings or even a referral.
✨Tip Number 2
Prepare for interviews by brushing up on your knowledge of GCP and regulatory requirements. We recommend practising common interview questions related to site management and trial execution to show you're the right fit for the role.
✨Tip Number 3
Don’t forget to showcase your interpersonal skills! During interviews, highlight your ability to engage effectively with sponsors and site staff. This is crucial in ensuring smooth communication throughout the monitoring lifecycle.
✨Tip Number 4
Apply directly through our website! It’s the best way to ensure your application gets noticed. Plus, it shows your enthusiasm for joining TFS HealthScience and contributing to innovative therapies in ophthalmology.
We think you need these skills to ace Senior Clinical Research Associate in City of Westminster
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your experience in ophthalmology and clinical trial monitoring. We want to see how your background aligns with the role, so don’t be shy about showcasing relevant skills and achievements!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you’re passionate about clinical research and how your values align with ours at TFS HealthScience. Keep it engaging and personal – we love a good story!
Showcase Your Interpersonal Skills: Since this role involves working closely with sponsors and site staff, make sure to highlight your strong interpersonal skills. We want to know how you build relationships and manage communication effectively in your application.
Apply Through Our Website: We encourage you to apply directly through our website for a smoother process. It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, it shows you’re keen on joining our team!
How to prepare for a job interview at TFS HealthScience
✨Know Your Ophthalmology Inside Out
Make sure you brush up on your ophthalmology knowledge before the interview. Familiarise yourself with the latest trends, challenges, and innovations in the field. This will not only show your passion but also demonstrate that you're ready to contribute meaningfully to the team.
✨Showcase Your Monitoring Experience
Be prepared to discuss your previous clinical trial monitoring experiences in detail. Highlight specific examples where you ensured adherence to protocols and regulatory requirements. This is your chance to shine a light on your skills and how they align with the role's responsibilities.
✨Engage with the Interviewers
Remember, interviews are a two-way street! Prepare thoughtful questions about TFS HealthScience’s approach to clinical trials and their values. This shows that you’re genuinely interested in the company and its mission, and it helps you assess if it’s the right fit for you.
✨Demonstrate Your Problem-Solving Skills
Since the role involves implementing risk-based approaches, be ready to discuss how you've proactively resolved issues in past projects. Use specific examples to illustrate your critical thinking and adaptability, which are crucial for maintaining trial quality.