Find a job 
Featured Companies 
Featured Universities 
For Companies At a Glance
- Tasks: Lead and manage clinical trials, ensuring success and timely delivery.
- Company: Join a leading organisation in clinical research with a global impact.
- Benefits: Competitive salary, flexible working options, and opportunities for professional growth.
- Why this job: Make a difference in healthcare by driving innovative clinical trials.
- Qualifications: Strong project management skills and experience in clinical trials, preferably in Oncology or Immunology.
- Other info: Dynamic team environment with a focus on collaboration and high performance.
The predicted salary is between 36000 - 60000 £ per year.
The CTL provides leadership and direction to the trial team and is accountable for the overall success and delivery of their assigned clinical trial according to defined milestones and KPI’s. They are responsible for steering and directing clinical trial activities, including patient and site engagement activities, direct communication and interaction with multiple internal and external stakeholders, and team members on a global, multi-country or regional basis.
The CTL is responsible for managing the planning, implementation and tracking of the clinical trial processes as well as risk mitigation. The CTL serves as a proactive member of the Clinical delivery team, liaising closely with the CTM on all study related issues, as Lead of the Trial team the CTL communicates trial status to all shareholders.
Accountabilities- Trial Preparation
- Accountable for the accurate planning and operational feasibility of trial timelines; and oversight of trial preparation to ensure trial team members are aligned and on track.
- Supports development of trial level documents owned by other functions (e.g. Statistics, Data Management, Study Physician, Medical Writing, Site Monitoring).
- Verifies and provides input into the country allocation and oversees trial feasibility.
- Accountable for development and implementation of trial level engagement plans, recruitment planning and risk mitigation.
- Leads development of core trial and patient facing documents.
- Integrates patient site level feedback during document development and ensures trials are designed with a focus on patient value.
- Ensures activities are front loaded where possible at the trial level and cascaded to country level to facilitate efficiencies as well as to ensure leverage and speed.
- Oversees outsourcing of vendor services in conjunction with other functions.
- Supports identification of vendors, vendor selection and development of vendor scope of work.
- Works with functional partners to ensure that all required trial processes are in place to meet trial delivery milestones (e.g. clinical quality monitoring, safety monitoring and reporting, investigational medicinal product, trial budget, site monitoring).
- Aligns and supports team members in timely responses to questions from the RA/EC and other external stakeholders.
- Provides/supports provision of appropriate study specific and standardized non-trial specific trial team training, internal and external partners.
- Trial Conduct
- Maintains oversight during clinical trial conduct including adherence to GCP and all global and local regulatory requirements; compliance with SOPs and continuous risk monitoring/mitigation.
- In collaboration with other functions, ensures budget oversight, including support of regular clinical quality monitoring, SMC/DMC management and safety reporting.
- Prepare and implement amendments of core documents, including training material updates/retraining as needed.
- Support authority/ethics response to requests as applicable.
- Maintain oversight of outsourcing of vendor services (including Central Lab) in conjunction with other functions.
- Monitors progress of patient recruitment and accrual of endpoints and proactively update and action contingencies throughout trial conduct.
- For early clinical trials, coordinates and harmonizes innovation unit tasks in trial (e.g. biomarker sampling, genomics, sub-studies).
- Trial Closeout and Reporting
- In collaboration with other functions, ensures timely cleaning and delivery of clinical trial data.
- Coordinates and supports trial medical writer in providing the CTR.
- Responsible for timely, complete and compliant archiving of all relevant global documents in the TMF, including all required documents from vendors.
- Supports results/documents disclosure of global registries.
- May support publication of trial data.
- Strong clinical trial project management experience.
- In depth understanding of project management with an emphasis on teamwork, to promote high performance teams.
- Experience in either Oncology, CNS, Immunology or Vaccines.
- Extensive experience in clinical trial project management across international trials.
- Masters Degree ideal but not essential.
Clinical Trial Leader - FSP in London employer: Parexel International
Contact Detail:
Parexel International Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Clinical Trial Leader - FSP in London
✨Tip Number 1
Network like a pro! Reach out to your connections in the clinical trial space, attend industry events, and engage on platforms like LinkedIn. We all know that sometimes it’s not just what you know, but who you know that can help you land that dream job.
✨Tip Number 2
Prepare for interviews by brushing up on your knowledge of clinical trial processes and recent advancements in the field. We recommend practising common interview questions with a friend or even in front of the mirror. Confidence is key!
✨Tip Number 3
Showcase your leadership skills! During interviews, share specific examples of how you've successfully led teams or managed projects in the past. We want to see how you can steer a trial team to success!
✨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. Let’s get you that Clinical Trial Leader position!
We think you need these skills to ace Clinical Trial Leader - FSP in London
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Clinical Trial Leader role. Highlight your project management experience and any relevant clinical trial work you've done. We want to see how your skills align 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 trials and how you can contribute to our team. Keep it engaging and make it personal – we love to see your personality come through.
Showcase Teamwork Skills: Since this role involves leading a trial team, emphasise your teamwork and leadership experiences. Share examples of how you've successfully collaborated with others in past projects. We value strong team players!
Apply Through Our Website: Don't forget to apply 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 awesome team at StudySmarter!
How to prepare for a job interview at Parexel International
✨Know Your Clinical Trials Inside Out
Before the interview, make sure you thoroughly understand the clinical trial processes and the specific requirements of the role. Familiarise yourself with key terms like GCP, KPI, and risk mitigation. This will not only help you answer questions confidently but also demonstrate your genuine interest in the position.
✨Showcase Your Leadership Skills
As a Clinical Trial Leader, you'll need to steer teams effectively. Prepare examples from your past experiences where you've successfully led a team or managed a project. Highlight how you engaged stakeholders and ensured alignment among team members, as this is crucial for the role.
✨Prepare for Scenario-Based Questions
Expect to face scenario-based questions that assess your problem-solving skills and decision-making abilities. Think about potential challenges in clinical trials, such as patient recruitment issues or regulatory hurdles, and prepare your strategies for overcoming them.
✨Ask Insightful Questions
At the end of the interview, don’t forget to ask questions that show your enthusiasm for the role and the company. Inquire about their approach to patient engagement or how they measure success in clinical trials. This not only shows your interest but also helps you gauge if the company aligns with your values.
