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- Tasks: Monitor clinical trials, ensuring compliance and patient safety while mentoring junior team members.
- Company: Join Fortrea, a global leader in innovative clinical research.
- Benefits: Flexible career progression, collaborative environment, and opportunities for mentorship.
- Why this job: Make a real impact in advancing healthcare through cutting-edge clinical trials.
- Qualifications: Degree in life sciences and 2 years of relevant experience required.
- Other info: Exciting opportunities across the UK with a focus on growth and development.
The predicted salary is between 35000 - 45000 £ per year.
Are you looking to grow your career in clinical research? Fortrea is hiring CRAs at various seniority levels to join our dynamic team. We have opportunities across the UK, ideally in Scotland, the Midlands, and the South East, offering an exciting chance to work on diverse studies while ensuring compliance with regulatory guidelines and company SOPs.
Why Join Fortrea?
- Be part of a global, innovative organization driving advancements in clinical research.
- Work on cutting-edge trials across a range of therapeutic areas.
- Enjoy flexible career progression, with opportunities at different CRA levels.
- Benefit from a collaborative team environment that values mentorship and growth.
Key Responsibilities
- Conduct and oversee study site monitoring visits to ensure compliance with protocols and regulatory requirements.
- Manage all aspects of site activities, including site initiation, monitoring visits and closeouts.
- Ensure patient safety, data integrity, and adherence to GCP guidelines.
- Support feasibility assessments, investigator recruitment and vendor coordination.
- Mentor junior team members and contribute to quality control efforts.
- Track and report Serious Adverse Events (SAEs) as required.
Qualifications
- University/college degree in life sciences or a relevant allied health field.
- At least 2 years of experience in a related role (e.g., Site Management, CRA).
- Basic knowledge of Regulatory Guidelines and the clinical trial process.
- Strong communication, organizational, and problem-solving skills.
- A valid driver’s license and willingness to travel.
CRA II, client-dedicated in Thatcham employer: Fortrea
Contact Detail:
Fortrea Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land CRA II, client-dedicated in Thatcham
✨Tip Number 1
Network like a pro! Reach out to your connections in the clinical research field, attend industry events, and join relevant online groups. We all know that sometimes it’s not just what you know, but who you know that can help you land that CRA role.
✨Tip Number 2
Prepare for interviews by brushing up on your knowledge of regulatory guidelines and the clinical trial process. We recommend practising common interview questions with a friend or even in front of the mirror. Confidence is key, and knowing your stuff will help you shine!
✨Tip Number 3
Showcase your experience! When discussing your previous roles, highlight specific examples where you ensured compliance and contributed to patient safety. We want to see how you’ve made an impact in your past positions, so don’t hold back!
✨Tip Number 4
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. So, get your CV ready and let’s get you on board with Fortrea!
We think you need these skills to ace CRA II, client-dedicated in Thatcham
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the CRA II role. Highlight your relevant experience in clinical research and any specific skills that match the job description. We want to see how you fit into our dynamic team!
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 background aligns with Fortrea's mission. Let us know what excites you about this opportunity!
Showcase Your Skills: Don’t forget to highlight your communication, organisational, and problem-solving skills in your application. These are key for a CRA role, and we want to see examples of how you've used them in your previous work.
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’s super easy!
How to prepare for a job interview at Fortrea
✨Know Your Stuff
Make sure you brush up on your knowledge of clinical research and regulatory guidelines. Familiarise yourself with the specific protocols and compliance requirements relevant to the role at Fortrea. This will not only show your enthusiasm but also demonstrate that you're serious about the position.
✨Showcase Your Experience
Prepare to discuss your previous roles in site management or as a CRA. Highlight specific examples where you've ensured patient safety, maintained data integrity, or mentored junior team members. Use the STAR method (Situation, Task, Action, Result) to structure your answers effectively.
✨Ask Insightful Questions
Interviews are a two-way street! Prepare thoughtful questions about the team dynamics, mentorship opportunities, and the types of studies you'll be involved in. This shows that you're genuinely interested in the role and helps you assess if Fortrea is the right fit for you.
✨Be Ready to Discuss Challenges
Think about challenges you've faced in previous roles, especially related to site monitoring or regulatory compliance. Be prepared to discuss how you overcame these obstacles and what you learned from them. This will highlight your problem-solving skills and resilience, which are crucial for a CRA.