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- Tasks: Support Clinical Project Managers in delivering impactful clinical studies from start to finish.
- Company: Join a leading biopharmaceutical company dedicated to improving patient lives.
- Benefits: Competitive salary, flexible working options, and opportunities for professional growth.
- Other info: Dynamic work environment with a focus on collaboration and career advancement.
- Why this job: Be part of a team that drives innovation in clinical research and makes a real difference.
- Qualifications: Bachelor’s degree and 1-2 years in clinical research or project support.
The predicted salary is between 30000 - 40000 £ per year.
About the role
In this role, you will provide hands‑on operational support to a Clinical Project Manager to deliver clinical studies from protocol through final report and archiving of the trial master file. You will help keep plans, documents, systems, and partners aligned so timelines, quality, and regulatory requirements are met. You will also contribute ideas that improve how we work across teams and partners.
Who you’ll work with
You will be working in a team that partners closely with Clinical Project Managers, cross‑functional study colleagues, and external partners such as service providers and investigational sites. Together, you will coordinate study activities, keep stakeholders informed, and maintain study documentation and systems so the study team can make timely, quality decisions.
What you’ll do
- Keep the trial master file complete and ready for audit or inspection through routine reviews and follow‑up with document owners.
- Support the creation, review, and finalisation of study documents, including protocols, amendments, consent forms, plans, submissions, and study reports.
- Coordinate stakeholder communication, meetings, decisions, and action logs, and maintain accurate study contact lists and procedure references.
- Track study status, metrics, invoices, and risks, and share clear updates with the study team and leadership.
- Help coordinate external partners and sites, support training activities, and assist readiness for audits, inspections, and issue resolution.
- Set up and maintain study records in clinical systems, perform quality checks, and provide support for system questions from sites and partners.
Requirements
- Bachelor’s degree (or equivalent) in a relevant scientific, health, or business discipline.
- One to two years’ experience in clinical research, such as monitoring, trial coordination, or project support.
- Experience supporting clinical studies across phases one to four, including early development and post‑approval studies.
- Comfortable using office productivity tools and study systems, with strong attention to detail and data quality.
- Excellent written and spoken English, with clear, respectful communication across cultures and time zones.
- Strong organisation, prioritisation, and learning mindset; able to raise issues early and help find practical solutions.
Associate Clinical Project Manager (UK) in Slough employer: UCB S.A.
Contact Detail:
UCB S.A. Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Associate Clinical Project Manager (UK) in Slough
✨Tip Number 1
Network like a pro! Reach out to people in the industry, especially those already working at UCB. A friendly chat can open doors and give you insider info on what it’s really like to work there.
✨Tip Number 2
Prepare for interviews by knowing your stuff! Research UCB’s recent projects and be ready to discuss how your experience aligns with their goals. Show them you’re not just another candidate, but someone who genuinely cares about their mission.
✨Tip Number 3
Practice makes perfect! Do mock interviews with friends or use online resources to get comfortable with common questions. The more you practice, the more confident you’ll feel when it’s your turn to shine.
✨Tip Number 4
Don’t forget to follow up! After your interview, send a quick thank-you email to express your appreciation. It’s a nice touch that keeps you fresh in their minds and shows your enthusiasm for the role.
We think you need these skills to ace Associate Clinical Project Manager (UK) in Slough
Some tips for your application 🫡
Tailor Your CV: Make sure your CV reflects the skills and experiences that match the Associate Clinical Project Manager role. Highlight any relevant clinical research experience and be specific about your contributions in previous roles.
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you're passionate about clinical research and how your background makes you a great fit for our team. Don’t forget to mention how you can contribute to improving our processes!
Showcase Your Communication Skills: Since you'll be coordinating with various stakeholders, it's crucial to demonstrate your excellent written communication skills. Keep your application clear, concise, and professional, while still showing a bit of your personality.
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 the role. Plus, it shows you’re keen on joining our team at StudySmarter!
How to prepare for a job interview at UCB S.A.
✨Know Your Stuff
Make sure you understand the basics of clinical project management and the specific role you're applying for. Brush up on key terms, processes, and regulations related to clinical studies. This will help you answer questions confidently and show that you're genuinely interested in the position.
✨Showcase Your Experience
Prepare examples from your past experiences that highlight your skills in coordinating projects, managing documentation, and communicating with stakeholders. Use the STAR method (Situation, Task, Action, Result) to structure your answers and make them impactful.
✨Ask Smart Questions
At the end of the interview, have a few thoughtful questions ready about the team dynamics, project challenges, or how success is measured in this role. This not only shows your enthusiasm but also helps you gauge if the company is the right fit for you.
✨Be Organised
Before the interview, organise your thoughts, documents, and any questions you want to ask. Make sure you have a clear understanding of your own resume and be ready to discuss any part of it. Being organised will help you feel more confident and in control during the interview.