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- Tasks: Lead and manage CAR-T clinical trials while ensuring compliance and timely delivery.
- Company: Join Parexel, a leader in clinical research with a supportive culture.
- Benefits: Enjoy remote work flexibility, career development opportunities, and a friendly environment.
- Why this job: Make a real impact in healthcare by managing innovative clinical studies.
- Qualifications: 3+ years of clinical trial experience and CAR-T expertise required.
- Other info: Great prospects for career growth and skill development in a dynamic field.
The predicted salary is between 36000 - 60000 £ per year.
Clinical Trial Manager – CAR-T Experience Required – UK (Remote) – FSP – REGISTER YOUR INTEREST
Parexel Uxbridge, England, United Kingdom
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Clinical Trial Manager – CAR-T Experience Required – UK (Remote) – FSP – REGISTER YOUR INTEREST
Parexel Uxbridge, England, United Kingdom
1 day ago Be among the first 25 applicants
Join to apply for the Clinical Trial Manager – CAR-T Experience Required – UK (Remote) – FSP – REGISTER YOUR INTEREST role at Parexel
***REGISTER YOUR INTEREST FOR AN UPCOMING ROLE IN THE UK***
Parexel is currently seeking a Clinical Trial Manager with CAR-T experience to join us in the UK. You will be assigned to one of our key sponsors in the region.
Working as a Clinical Trial Manager at Parexel FSP offers tremendous long-term job security and prospects. We undertake vital clinical studies for sponsors including the leading global biotechs and Pharma top 50. And we have an incredible pipeline of work.
Whether you see your future path in fields such as clinical operations, project management, line management, or other positions, we have a world of opportunity waiting for you.
Our Clinical Trial Managers work from their home office base, supporting studies within their country or region. ‘Manageable sites, manageable protocols’ is our mantra. Expect exciting professional challenges in inspiring studies, but with time for your outside life.
Some Specifics About This Advertised Role
- Dedicated to one client.
- Responsible at country level to deliver committed components of clinical studies according to agreed resources, budget and timelines complying with Client Procedural Documents, international guidelines such as ICH-GCP as well as relevant local regulations.
- Ensures timely preparation of country financial Study Management Agreement (fSMA) and maintains accurate study budget in client clinical studies financial system by regular checks of the system and financial reports.
- Leads and optimizes the performance of the Local Study Team(s) at country level ensuring compliance with client Procedural Documents, ICH-GCP and local regulations.
- Ensures timely preparation of country level Master Informed Consent Form (MICF) and subsequent site level ICFs, as required, including any relevant translations, and in line with relevant client SOPs and local regulations.
- Ensures timely submission of application/documents to EC/IRB at start up and for the duration of the study.
Here are a few requirements specific to this advertised role.
- Minimum of 3 years\’ experience running local clinical trials.
- CAR-T experience is essential.
- Proven ability to lead and motivate cross functional teams to deliver clinical trials according to or ahead of time plan, budget and with required quality.
- Experience in, and willingness to monitor oncology clinical trials – if needed based on flexible capacity.
- Experience performing submissions to RA and EC
- Experience partnering with study functions to ensure smooth delivery.
- Effective time management, organizational and interpersonal skills & problem-solving skills, with the ability to multi-task and prioritize.
- Good understanding and working knowledge of clinical research, phases of clinical trials, current GCP/ICH & country clinical research law & guidelines.
We care about our people and your passion, as they are the key to our success, and provide an open and friendly work environment where we empower people and provide them with opportunities to develop their long-term careers. In addition, you will have the opportunity to develop within your role and tackle further responsibilities or develop your skill set within other related departments of Parexel.
Who Are Parexel
Parexel supports clinical studies across the full range of therapeutic areas, and we have longstanding partnerships with a vast client base.
We supported the trials of most of today’s top 50 best-selling drugs, but equally we enable more niche drug developments that are critical to the well-being of many patients.
You’ll be an influential member of the wider team.
Not quite the role for you?
Join Our Talent Community and we’ll reach out with job alerts when positions that match your career interests become available. We’ll also share periodic updates about the latest company news and events.
Sign up today https://jobs.parexel.com/functional-service-provider
Seniority level
-
Seniority level
Mid-Senior level
Employment type
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Employment type
Full-time
Job function
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Job function
Health Care Provider, Science, and Research
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Industries
Pharmaceutical Manufacturing, Biotechnology Research, and Hospitals and Health Care
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Clinical Trial Manager - CAR-T Experience Required - UK (Remote) - FSP - REGISTER YOUR INTEREST employer: Parexel
Contact Detail:
Parexel Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Clinical Trial Manager - CAR-T Experience Required - UK (Remote) - FSP - REGISTER YOUR INTEREST
✨Tip Number 1
Network like a pro! Reach out to your connections in the clinical trial space, especially those with CAR-T experience. A friendly chat can lead to insider info about job openings or even referrals.
✨Tip Number 2
Prepare for virtual interviews by practising common questions and showcasing your CAR-T expertise. We recommend setting up a mock interview with a friend to get comfortable with the format.
✨Tip Number 3
Don’t forget to follow up after interviews! A quick thank-you email can keep you top of mind and show your enthusiasm for the role. Plus, it’s a great chance to reiterate your passion for clinical trials.
✨Tip Number 4
Keep an eye on our website for new opportunities! We’re always updating our listings, and applying directly through us can give you a better shot at landing that Clinical Trial Manager role.
We think you need these skills to ace Clinical Trial Manager - CAR-T Experience Required - UK (Remote) - FSP - REGISTER YOUR INTEREST
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to highlight your CAR-T experience and relevant clinical trial management skills. We want to see how your background aligns with the role, so don’t hold back on showcasing your achievements!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to tell us why you’re passionate about clinical trials and how your experience makes you the perfect fit for this role. Keep it engaging and personal – we love a good story!
Showcase Your Team Leadership Skills: Since leading cross-functional teams is key in this role, make sure to highlight any relevant experiences where you’ve successfully motivated and guided teams. We’re looking for those standout moments that demonstrate your leadership prowess!
Apply Through Our Website: Don’t forget to apply through our website! It’s the best way to ensure your application gets into the right hands. Plus, it gives you a chance to explore more about us and what we stand for at Parexel.
How to prepare for a job interview at Parexel
✨Know Your CAR-T Stuff
Make sure you brush up on your CAR-T knowledge before the interview. Be ready to discuss your experience in detail, including specific trials you've managed and any challenges you've faced. This will show that you're not just familiar with the terminology but have real-world experience.
✨Showcase Your Leadership Skills
As a Clinical Trial Manager, you'll need to lead cross-functional teams. Prepare examples of how you've motivated teams in the past, resolved conflicts, or improved team performance. Use the STAR method (Situation, Task, Action, Result) to structure your responses.
✨Understand the Regulatory Landscape
Familiarise yourself with ICH-GCP guidelines and local regulations relevant to clinical trials. Be prepared to discuss how you've ensured compliance in previous roles. This demonstrates your commitment to quality and safety in clinical research.
✨Ask Insightful Questions
Interviews are a two-way street! Prepare thoughtful questions about the company's approach to clinical trials, their client relationships, and future projects. This shows your genuine interest in the role and helps you assess if it's the right fit for you.