Find a job 
Featured Companies 
Featured Universities 
For Companies At a Glance
- Tasks: Lead and manage Phase 3 clinical trials, ensuring compliance and effective project execution.
- Company: Join a high-calibre team at a pivotal moment in clinical research.
- Benefits: Competitive salary, professional development, and the chance to make a real impact.
- Why this job: Be at the forefront of innovative therapies and drive meaningful change in healthcare.
- Qualifications: 8+ years in clinical research with proven trial management experience.
- Other info: Dynamic environment with opportunities for growth in a crucial therapeutic area.
The predicted salary is between 60000 - 80000 £ per year.
Their lead programme is entering Phase 3, a significant inflection point for both the asset and the organisation. This is a rare opportunity to join a focused, high-calibre team at the moment it matters most: building the clinical infrastructure to take a differentiated therapy through a pivotal global trial.
As Senior/Clinical Trial Manager, you will own end-to-end execution of one or more Phase 3 studies.
- Lead the creation and management of study project plans timelines, budgets, resourcing, and vendor coordination from concept through final CSR.
- Serve as the primary sponsor-side operational lead for CRO oversight, including governance cadence, KPI tracking, and performance management.
- Ensure all trials are conducted in compliance with ICH-GCP, FDA, EMA, MHRA, and applicable local regulations across multiple jurisdictions.
- Drive proactive risk identification and mitigation owning the risk register and escalating appropriately to the medical monitor and VP.
- Manage IP logistics, clinical lab samples, and ancillary supply shipments across US and European sites.
- Review SAEs and pertinent safety data with the medical monitor and drug safety team to identify trends and signals.
- Ensure ongoing compilation, organisation, and reconciliation of the Trial Master File.
8+ years of clinical research experience in an industry (sponsor-side) setting.
Minimum 3 years as a project lead or trial manager, with clear ownership of Phase 2/3 trial execution.
Proven CRO management track record: governance, SLAs, performance escalation.
Strong working knowledge of GCP, ICH guidelines, and multi-jurisdictional regulatory requirements.
Experience with TMF management, budget tracking, and trial tools (SmartSheet, MS Project, Veeva, Medidata or similar).
Therapeutic area experience in metabolic disease, hepatology, GI, or cardiometabolic strongly preferred.
Locations
Clinical Trial Manager (Permanent) in Basildon, Essex employer: LumaBio Partners
Contact Detail:
LumaBio Partners Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Clinical Trial Manager (Permanent) in Basildon, Essex
✨Tip Number 1
Network like a pro! Reach out to your connections in the clinical research field, especially those who have experience with Phase 3 trials. A friendly chat can lead to insider info about job openings or even referrals.
✨Tip Number 2
Prepare for interviews by brushing up on your knowledge of ICH-GCP and regulatory requirements. We want you to be ready to discuss how you've managed trials and handled CRO oversight. Show them you know your stuff!
✨Tip Number 3
Don’t just apply anywhere; focus on companies that align with your experience in metabolic disease or hepatology. Tailor your approach to highlight your relevant skills and experiences that match their needs.
✨Tip Number 4
Use our website to apply directly! It’s the best way to ensure your application gets noticed. Plus, we’re always looking for passionate individuals who can help us drive clinical trials forward.
We think you need these skills to ace Clinical Trial Manager (Permanent) in Basildon, Essex
Some tips for your application 🫡
Tailor Your CV: Make sure your CV reflects the specific skills and experiences that match the Clinical Trial Manager role. Highlight your project management experience, especially in Phase 2/3 trials, and any relevant therapeutic area expertise.
Craft a Compelling Cover Letter: Use your cover letter to tell us why you're the perfect fit for this role. Share your passion for clinical research and how your background aligns with our mission to take differentiated therapies through pivotal global trials.
Showcase Your CRO Management Skills: Since CRO oversight is key for this position, be sure to detail your experience managing CROs. Talk about your governance practices, KPI tracking, and how you've handled performance management in past roles.
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 this exciting opportunity at such a crucial time for our lead programme.
How to prepare for a job interview at LumaBio Partners
✨Know Your Stuff
Make sure you brush up on the specifics of clinical trial management, especially Phase 3 studies. Familiarise yourself with ICH-GCP guidelines and the regulatory requirements for the jurisdictions involved. This will show that you're not just a candidate, but someone who truly understands the landscape.
✨Showcase Your Experience
Prepare to discuss your previous roles in detail, particularly your experience as a project lead or trial manager. Highlight specific examples where you successfully managed timelines, budgets, and vendor coordination. This is your chance to demonstrate your proven track record in CRO management.
✨Be Ready for Scenario Questions
Expect questions that put you in hypothetical situations related to risk management and problem-solving. Think about how you would proactively identify risks and what steps you would take to mitigate them. Having a few scenarios prepared can really set you apart.
✨Ask Insightful Questions
At the end of the interview, don’t shy away from asking questions. Inquire about the team dynamics, the specific challenges they face in the current Phase 3 study, or how they measure success in their trials. This shows your genuine interest and helps you gauge if the company is the right fit for you.