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- Tasks: Manage clinical trial budgets, staff, and data integrity while ensuring compliance with regulations.
- Company: Join a global leader in life sciences research and technology with a focus on AI-driven solutions.
- Benefits: Enjoy a hybrid work model with competitive pay of £30.08 per hour PAYE.
- Why this job: Be part of innovative projects that optimise healthcare outcomes and make a real impact.
- Qualifications: 5+ years in clinical trial management with strong budgeting and ethics knowledge required.
- Other info: Must have the right to work in the UK; DBS check may be needed.
The predicted salary is between 60000 - 84000 £ per year.
CK Group are recruiting for a Clinical Project Manager, to join a leading provider of advanced analytics research and technology solutions to the life sciences industry, at their site based in Paddington, London, Basildon, and working from home, on a contract basis for 12 months. This role is a hybrid position. Rate: £30.08 per hour PAYE.
Clinical Project Manager Role:
- Overseeing the budget for clinical trials and ensuring that resources are allocated appropriately, including managing staff, equipment, and supplies, as well as monitoring expenses and identifying cost-saving measures.
- Recruiting, training, and supervising vendor/staff, including clinical research associates and data managers. Ensure that vendor/staff are properly trained on study protocols and that they follow GCP guidelines and other regulatory requirements.
- Ensuring the integrity and accuracy of clinical trial data by overseeing data management activities, including data collection, analysis, and reporting as well as ensuring that data is stored securely and in compliance with regulatory requirements.
- Developing and implementing quality control measures to ensure compliance with regulatory requirements and standards.
- Liaising with study CROs, principal investigators, and other stakeholders to provide regular updates on study progress and to address any issues or concerns that arise during the course of the study.
Your Background:
- Knowledge of budgeting and tracking.
- Strong knowledge of safety and ethics.
- Ability to coordinate site management with research activities.
- Experience within outsourcing and contracts within the Pharmaceutical industry is preferred or at least demonstrable knowledge of contracts, bid meetings and negotiations.
- Minimum 5+ years of experience in clinical trial management.
- Detail-oriented, analytical, and able to work effectively in a team environment.
Company: Our client offers research services and technology solutions in the life sciences industry. With just under 100,000 employees, the company has operations in over 90 countries worldwide. Our client’s ambitions involve optimising results of innovations using artificial intelligence.
Location: This role is a hybrid role, it is based at our client’s site in Paddington, London and also Basildon.
Apply: It is essential that applicants hold entitlement to work in the UK. Please quote job reference 123 937 in all correspondence. Please note: This role may be subject to a satisfactory basic Disclosure and Barring Service (DBS) check.
If this position isn’t suitable but you are looking for a new role, or if you are interested in seeing what opportunities are out there, head over to our LinkedIn page (cka-group) and follow us to see our latest jobs and company news.
Clinical Trial Manager employer: CK Group
Contact Detail:
CK Group Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Clinical Trial Manager
✨Tip Number 1
Familiarise yourself with the latest trends in clinical trial management, especially regarding budgeting and resource allocation. This knowledge will help you speak confidently about your experience and how it aligns with the role during any discussions.
✨Tip Number 2
Network with professionals in the life sciences industry, particularly those who have experience in clinical project management. Engaging with them can provide insights into the company culture and expectations, which can be invaluable during interviews.
✨Tip Number 3
Prepare to discuss specific examples of how you've managed clinical trials in the past, focusing on your ability to oversee budgets and ensure compliance with regulatory requirements. Real-life scenarios can demonstrate your expertise effectively.
✨Tip Number 4
Stay updated on GCP guidelines and other regulatory requirements relevant to clinical trials. Being well-versed in these areas will not only boost your confidence but also show potential employers that you're committed to maintaining high standards in your work.
We think you need these skills to ace Clinical Trial Manager
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights relevant experience in clinical trial management, particularly focusing on budgeting, staff management, and compliance with GCP guidelines. Use specific examples to demonstrate your skills.
Craft a Strong Cover Letter: Write a cover letter that addresses the key responsibilities of the Clinical Project Manager role. Mention your experience with vendor management and your understanding of regulatory requirements, showcasing how you can contribute to the company's goals.
Highlight Relevant Experience: In your application, emphasise your 5+ years of experience in clinical trial management. Include details about your previous roles, especially those involving budget oversight and team coordination, to show you meet the job requirements.
Follow Application Instructions: Ensure you quote the job reference number (123 937) in all correspondence and confirm your entitlement to work in the UK. This attention to detail can set you apart from other candidates.
How to prepare for a job interview at CK Group
✨Understand the Role Thoroughly
Before your interview, make sure you have a solid understanding of the Clinical Project Manager role. Familiarise yourself with the responsibilities such as budget management, staff supervision, and data integrity. This will help you answer questions confidently and demonstrate your suitability for the position.
✨Showcase Your Experience
Highlight your relevant experience in clinical trial management, especially your knowledge of budgeting, safety, and ethics. Be prepared to discuss specific examples from your past roles that showcase your ability to manage resources effectively and ensure compliance with regulatory requirements.
✨Prepare Questions for the Interviewers
Having insightful questions ready shows your interest in the role and the company. Ask about their approach to using artificial intelligence in clinical trials or how they handle challenges in project management. This not only demonstrates your enthusiasm but also helps you gauge if the company aligns with your career goals.
✨Emphasise Team Collaboration
Since the role involves liaising with various stakeholders, emphasise your ability to work effectively in a team environment. Share examples of how you've successfully collaborated with clinical research associates, vendors, and other team members to achieve project goals.
