At a Glance
- Tasks: Support clinical trials in London, ensuring compliance and data quality.
- Company: Join a leading global pharmaceutical company dedicated to innovation.
- Benefits: Flexible part-time hours, personal growth opportunities, and a collaborative team environment.
- Other info: Ideal for those seeking part-time work with impactful responsibilities.
- Why this job: Make a real difference in patients' lives while gaining valuable experience.
- Qualifications: Experience as a CRA and strong knowledge of GCP and trial processes.
The predicted salary is between 30000 - 40000 £ per year.
About the role
The Clinical Research Associate (CRA) is responsible for supporting clinical trial activities at a single site in London. The role ensures that the study is conducted in accordance with protocol, GCP and regulatory requirements. This is a part‑time position with limited site oversight. As part of our SRS FSP team, the CRA will be dedicated to one sponsor – a global pharmaceutical or biotechnology company that is an industry leader within its therapeutic area.
Key Responsibilities
- Perform site monitoring visits as required for one site in London
- Ensure compliance with study protocol, GCP and applicable regulatory requirements
- Act as the main point of contact for site staff
- Support site documentation review including TMF and essential documents
- Perform source data verification and ensure data quality
- Collaborate with the wider study team to support smooth study execution
Qualifications
- Previous experience as a CRA with independent monitoring responsibilities
- Strong knowledge of GCP and clinical trial processes
- Experience with onsite monitoring activities
- Ability to work part time on a 0.1 FTE basis
- Based in or able to travel to London
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.
Clinical Research Associate - Freelance - 0.1FTE employer: TFS HealthScience
As a Clinical Research Associate with our SRS FSP team, you will be part of a dynamic and supportive work culture that prioritises collaboration and quality in clinical research. Located in London, this part-time role offers flexibility while allowing you to contribute to impactful studies for a leading global pharmaceutical company, ensuring your professional growth in a rewarding environment dedicated to improving patient outcomes.
StudySmarter Expert Advice🤫
We think this is how you could land Clinical Research Associate - Freelance - 0.1FTE
✨Tip Number 1
Network like a pro! Reach out to your connections in the clinical research field, especially those who might know about freelance opportunities. A friendly chat can lead to job leads that aren’t even advertised!
✨Tip Number 2
Prepare for interviews by brushing up on your GCP knowledge and clinical trial processes. We recommend practising common interview questions with a friend or in front of a mirror to boost your confidence.
✨Tip Number 3
Showcase your experience! When you get the chance to speak with potential employers, highlight your previous CRA roles and any independent monitoring responsibilities you've had. Make sure they see how you can add value to their team.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, we love seeing candidates who are proactive about their job search.
We think you need these skills to ace Clinical Research Associate - Freelance - 0.1FTE
Some tips for your application 🫡
Tailor Your CV:Make sure your CV highlights your experience as a CRA and any relevant monitoring responsibilities. We want to see how your skills align with the role, so don’t be shy about showcasing your knowledge of GCP and clinical trial processes!
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 previous experiences make you a great fit for our team. Keep it concise but impactful – we love a good story!
Showcase Your Attention to Detail:As a CRA, attention to detail is key. In your application, highlight specific examples where your meticulous nature has led to successful outcomes in past roles. This will show us that you understand the importance of compliance and data quality.
Apply Through Our Website:We encourage you to apply directly through our website. It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, it gives you a chance to explore more about what we do at StudySmarter!
How to prepare for a job interview at TFS HealthScience
✨Know Your GCP Inside Out
As a Clinical Research Associate, you'll need to demonstrate a solid understanding of Good Clinical Practice (GCP). Brush up on the latest guidelines and be ready to discuss how you've applied them in your previous roles. This shows you're not just familiar with the theory but can also implement it effectively.
✨Showcase Your Monitoring Experience
Be prepared to talk about your past experiences with site monitoring. Highlight specific examples where you ensured compliance with study protocols and regulatory requirements. This will help the interviewers see that you have the hands-on experience they’re looking for.
✨Emphasise Your Communication Skills
As the main point of contact for site staff, strong communication skills are essential. Think of examples where you successfully collaborated with a team or resolved conflicts. This will illustrate your ability to work well with others and support smooth study execution.
✨Prepare Questions About the Role
Interviews are a two-way street! Prepare thoughtful questions about the role, the team, and the company’s approach to clinical trials. This not only shows your interest but also helps you determine if this is the right fit for you.
