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- Tasks: Manage clinical trials and collaborate with vendors to ensure successful study execution.
- Company: Join Advanced Clinical, a leader in innovative clinical research.
- Benefits: Competitive salary, travel opportunities, and a supportive team environment.
- Other info: Dynamic role with opportunities for professional growth and collaboration.
- Why this job: Make a real impact in oncology research while developing your career.
- Qualifications: 5 years in clinical studies and strong communication skills required.
The predicted salary is between 36000 - 60000 £ per year.
Advanced Clinical is seeking an experienced Clinical Trial Manager to join our UK-based Functional Service Provider (FSP) team. This role will support global clinical studies and requires strong operational, vendor management, and monitoring oversight experience.
Responsibilities include:
- Managing external vendors and CROs
- Preparing key study documents, including Monitoring Manuals, Study Operations Manuals, SDV Plans, and Laboratory Manuals
- Designing and coordinating study materials such as CRFs, patient diaries, source documents, and participation cards
- Assisting with protocol development and study reports
- Overseeing monitoring activities to ensure compliance with GCP, SOPs, and study protocols
- Providing direction and support to CRAs
- Tracking patient enrollment, conducting site qualification/initiation/close-out activities, and supporting data management coordination
- Managing study supplies and negotiating vendor contracts
- Reviewing ICFs, CRFs, and study-related materials
- Planning and participating in investigator meetings
- Supporting the data query process
- Ensuring regulatory compliance and maintaining an up-to-date Trial Master File
Essential Requirements:
- BA/BS degree or nursing qualification (science preferred)
- Minimum 5 years' experience in clinical studies, including at least 1 year of site management
- Previous monitoring or study coordination experience preferred
- Strong knowledge of GCP and SOPs
- Understanding of clinical study phases
- Ability to work independently and within cross-functional teams
- Advanced proficiency in Word, Excel, and PowerPoint
- Experience with electronic systems such as TMF, CTMS, Veeva Vault, Smartsheet, and SharePoint
- Strong communication skills
- Willingness to travel 10–20%
To express interest or learn more about this opportunity, please get in touch. Advanced Clinical offers a collaborative environment where your contributions directly support the success of innovative clinical research.
Locations
Clinical Trial Manager in Cheshire, Warrington employer: Advanced Clinical
Contact Detail:
Advanced Clinical Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Clinical Trial Manager in Cheshire, Warrington
✨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 hunt for a Clinical Trial Manager role. You never know who might have the inside scoop on job openings or can put in a good word for you.
✨Tip Number 2
Get your LinkedIn game on point! Make sure your profile is up-to-date and showcases your experience in managing clinical trials. Join relevant groups and engage with posts to increase your visibility in the industry.
✨Tip Number 3
Prepare for interviews by brushing up on your knowledge of GCP and SOPs. Be ready to discuss your previous experiences with vendor management and monitoring oversight, as these are key skills for the Clinical Trial Manager role.
✨Tip Number 4
Don’t forget to check out our website for the latest job openings! Applying directly through us not only shows your interest but also gives you a better chance of landing that dream job in clinical trials.
We think you need these skills to ace Clinical Trial Manager in Cheshire, Warrington
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Clinical Trial Manager role. Highlight your experience in managing vendors, preparing study documents, and any relevant operational skills. We want to see how your background aligns with what we're looking for!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you're passionate about clinical trials and how your skills can contribute to our team. Keep it concise but impactful – we love a good story!
Showcase Your Experience: When detailing your experience, focus on specific achievements in clinical studies. Mention any successful projects you've led or challenges you've overcome. We appreciate candidates who can demonstrate their impact!
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 shows you’re keen on joining our team!
How to prepare for a job interview at Advanced Clinical
✨Know Your Stuff
Make sure you brush up on your knowledge of GCP, SOPs, and the clinical trial phases. Being able to discuss these topics confidently will show that you're not just familiar with the basics but also understand the intricacies of the role.
✨Vendor Management Insights
Since managing external vendors is a key part of the job, prepare examples from your past experiences where you successfully handled vendor relationships. Highlight any challenges you faced and how you overcame them to demonstrate your problem-solving skills.
✨Showcase Your Documentation Skills
Be ready to talk about your experience in preparing study documents like Monitoring Manuals and Study Operations Manuals. Bring along samples or be prepared to discuss how you ensure compliance and accuracy in your documentation.
✨Ask Smart Questions
Prepare thoughtful questions about the company's approach to clinical trials and their expectations for the Clinical Trial Manager role. This shows your genuine interest in the position and helps you assess if it's the right fit for you.