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- Tasks: Lead clinical trial operations and ensure compliance across protocols.
- Company: Dynamic healthcare company focused on innovative clinical research.
- Benefits: Hybrid work model, competitive salary, and opportunities for professional growth.
- Why this job: Make a real impact on clinical development and patient outcomes.
- Qualifications: 6–8 years in clinical research with strong leadership skills.
- Other info: Collaborative environment with a focus on quality and compliance.
The predicted salary is between 60000 - 75000 £ per year.
Location: London (Hybrid) - 2–3 days/week on-site
We’re looking for an experienced Clinical Research Manager to lead country-level clinical trial operations. You’ll ensure performance, quality, and compliance across assigned protocols, manage vendors and sites, and collaborate with internal teams (PV, Regulatory, GMA, GHH). This is a customer-facing role with significant impact on trial delivery and country commitments.
Key Responsibilities- Oversee protocol execution, timelines, and budgets
- Ensure compliance with ICH-GCP and local regulations
- Lead quality oversight and training for CRAs/CTCs
- Build strong relationships with investigators and vendors
- Contribute to local and regional strategy
- 6–8 years’ clinical research experience (pharma/CRO/healthcare)
- Strong knowledge of ICH-GCP and drug development
- Excellent communication and leadership skills
- Ability to manage multiple protocols and stakeholders
- London-based, on-site 2–3 days/week
Apply now and make an impact on the future of clinical development!
Clinical Research Manager - Hybrid Trials & Compliance in Maidenhead employer: Fortrea
Contact Detail:
Fortrea Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Clinical Research Manager - Hybrid Trials & Compliance in Maidenhead
✨Tip Number 1
Network like a pro! Reach out to your connections in the clinical research field and let them know you're on the lookout for opportunities. You never know who might have a lead or can put in a good word for you.
✨Tip Number 2
Prepare for interviews by brushing up on your knowledge of ICH-GCP and local regulations. Be ready to discuss how you've ensured compliance and quality in past roles, as this will show you're the right fit for the Clinical Research Manager position.
✨Tip Number 3
Showcase your leadership skills! Think of examples where you've successfully managed teams or projects. This is key for a role that involves overseeing CRAs/CTCs and building relationships with vendors and investigators.
✨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 Manager - Hybrid Trials & Compliance in Maidenhead
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Clinical Research Manager role. Highlight your experience in managing clinical trials, compliance, and any relevant leadership roles you've held. We want to see how your background aligns with our needs!
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 skills can contribute to our team. Be sure to mention your knowledge of ICH-GCP and your experience with vendor management.
Showcase Your Communication Skills: Since this role involves significant interaction with stakeholders, make sure to demonstrate your excellent communication skills in your application. Whether it's through your writing style or examples of past collaborations, we want to see how you connect with others.
Apply Through Our Website: We encourage you to apply directly through our website for the best chance of getting noticed. It’s super easy, and you’ll be able to keep track of your application status. Plus, we love seeing applications come in through our own platform!
How to prepare for a job interview at Fortrea
✨Know Your Protocols
Make sure you’re well-versed in ICH-GCP guidelines and the specific protocols relevant to the role. Brush up on your knowledge of compliance and quality oversight, as these will be key discussion points during the interview.
✨Showcase Your Leadership Skills
Prepare examples that highlight your leadership experience, especially in managing clinical trials and teams. Think about times when you successfully led a project or trained others, as this will demonstrate your capability to lead CRAs and CTCs effectively.
✨Build Relationships
Since this role involves significant interaction with investigators and vendors, be ready to discuss how you’ve built strong professional relationships in the past. Share specific strategies you’ve used to foster collaboration and trust.
✨Be Ready for Scenario Questions
Expect scenario-based questions that assess your problem-solving skills and ability to manage multiple protocols. Prepare to discuss how you would handle challenges related to timelines, budgets, or compliance issues in a clinical trial setting.