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- Tasks: Facilitate clinical trial documentation and approvals while ensuring compliance with regulations.
- Company: Join a leading collaboration in clinical research with top NHS and academic institutions.
- Benefits: Full-time role with an indefinite contract and opportunities for professional growth.
- Why this job: Make a real difference in healthcare by supporting innovative clinical trials.
- Qualifications: Strong organisational skills and a passion for clinical research are essential.
- Other info: Dynamic work environment with a focus on collaboration and quality.
The predicted salary is between 36000 - 60000 £ per year.
About us
The King’s Health Partners Clinical Trials Office (KHP-CTO) is a collaboration between King’s College London, Guy’s and St Thomas’ NHS Foundation Trust, King’s College Hospital NHS Foundation Trust and South London and Maudsley NHS Foundation Trust. Established to provide a single interface for those wishing to conduct clinical research within the partner organisations, and to ensure that there are common, efficient processes for the set up and administration of clinical trials.
About the role
- Facilitate the collection and preparation of documentation required to confirm local capacity, obtain R&D theme lead approvals, collate regulatory approvals needed to instigate clinical trials.
- Facilitate the collection of local and regulatory approvals required for the review and implementation of amendments.
- Provide comprehensive advice to external and internal parties for the conduct of clinical trials across the partner organisations.
- Assist in maintaining the records of the clinical trials portfolios of the partner organisations including the EDGE system and ensuring information added is quality checked.
- Ensure that trials metrics are collected to permit tracking of milestones.
- Assist in the archiving of clinical trials documentation to meet prevailing regulatory requirements.
- Maintain a working knowledge of prevailing regulations, guidance, best practices and GCP standards regarding the conduct of clinical trials.
- Ensure confidentiality of commercially sensitive information and that data protection imperatives are respected.
The above list of responsibilities may not be exhaustive, and the post holder will be required to undertake such tasks and responsibilities as may reasonably be expected within the scope and grading of the post.
This is a full time (35 hours per week), and you will be offered an indefinite contract.
Commercial Trials Facilitator - Strand, London, WC2R 2LS employer: King's College London
Contact Detail:
King's College London Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Commercial Trials Facilitator - Strand, London, WC2R 2LS
✨Tip Number 1
Network like a pro! Reach out to people in the industry, attend events, and connect with professionals on LinkedIn. You never know who might have the inside scoop on job openings or can put in a good word for you.
✨Tip Number 2
Prepare for interviews by researching the company and role thoroughly. Understand their values and how your skills align with their needs. Practise common interview questions and think of examples that showcase your experience in clinical trials.
✨Tip Number 3
Follow up after interviews! A simple thank-you email can go a long way in showing your enthusiasm for the role. It keeps you on their radar and demonstrates your professionalism.
✨Tip Number 4
Don’t forget to apply through our website! We’ve got loads of opportunities waiting for you, and applying directly can sometimes give you an edge over other candidates. Plus, it’s super easy!
We think you need these skills to ace Commercial Trials Facilitator - Strand, London, WC2R 2LS
Some tips for your application 🫡
Tailor Your Application: Make sure to customise your CV and cover letter for the Commercial Trials Facilitator role. Highlight your relevant experience in clinical trials and any specific skills that match the job description. We want to see how you fit into our team!
Showcase Your Knowledge: Demonstrate your understanding of clinical trial processes and regulations in your application. Mention any experience with documentation, approvals, or metrics tracking. This will show us that you're ready to hit the ground running!
Be Clear and Concise: When writing your application, keep it straightforward and to the point. Use clear language and avoid jargon unless it's relevant. We appreciate a well-structured application that’s easy to read!
Apply Through Our Website: Don’t forget to submit your application through our official website. It’s the best way for us to receive your details and ensures you’re considered for the role. We can’t wait to hear from you!
How to prepare for a job interview at King's College London
✨Know Your Stuff
Make sure you brush up on the latest regulations and best practices in clinical trials. Familiarise yourself with GCP standards and any recent changes in legislation that might affect the role. This will show your interviewers that you're not just interested, but also knowledgeable.
✨Showcase Your Organisational Skills
As a Commercial Trials Facilitator, you'll need to juggle multiple tasks. Prepare examples from your past experiences where you've successfully managed documentation or facilitated approvals. Highlight how you kept everything organised and on track, as this is crucial for the role.
✨Communicate Clearly
You'll be providing advice to various parties, so practice articulating complex information in a simple way. During the interview, demonstrate your ability to communicate effectively by answering questions clearly and concisely. This will help build confidence in your communication skills.
✨Emphasise Teamwork
This role involves collaboration across multiple organisations. Be ready to discuss how you've worked in teams before, especially in high-pressure situations. Share specific examples of how you contributed to team success and maintained confidentiality, as this is key in clinical trials.
