At a Glance
- Tasks: Lead risk management for clinical trials, ensuring patient safety and compliance.
- Company: Bristol Myers Squibb, a purpose-driven company transforming lives through innovative medicines.
- Benefits: Impactful work, career growth, supportive environment, and comprehensive benefits.
- Other info: Collaborative global team with opportunities for mentorship and professional networking.
- Why this job: Shape the future of clinical research while making a real difference for patients.
- Qualifications: 8+ years in clinical trial operations or GCP compliance, strong risk management skills.
The predicted salary is between 72000 - 88000 £ per year.
At Bristol Myers Squibb, our employees often ask, “Who are you working for?”—a question that fuels collaboration, accountability, and urgency in our work.
Our purpose-driven culture inspires us to discover, develop, and deliver innovative medicines to prevail over serious diseases.
We offer uniquely interesting and meaningful work, opportunities for growth, and a supportive environment that values inclusion, wellbeing, flexibility, and comprehensive benefits.
This is work that transforms the lives of patients, and the careers of those who do it.
Bristol Myers Squibb | Global Drug Development | Trial Risk & Integrity Management
What if your expertise could protect the integrity of clinical trials and the patients depending on them?
At Bristol Myers Squibb, we're on a mission to transform patients' lives through science.
And behind every successful clinical trial is a team of brilliant people making sure the work is done right, done safely, and done with integrity.
That's where you come in.
- We're looking for an
- Associate Director, Business Risk Management Lead (EU) to join our
- Trial Risk and Integrity Management (TRIM) team in
- Uxbridge, UK
- a role where your instinct for risk, your passion for quality and your ability to influence people at every level will directly shape the future of clinical research.
This isn't just a compliance role. It's a leadership platform.
You won't be ticking boxes or writing reports that gather dust.
You'll be the person who sees risks before they become problems and who builds the culture, the tools, and the confidence across teams to stay ahead of them.
You'll work at the intersection of science, strategy, and people, touching global clinical programmes that matter.
- Here's What That Looks Like In Practice
- You'll lead quality risk management end-to-end - identifying, assessing, and mitigating the risks that could threaten GCP compliance, clinical trial delivery and inspection readiness.
Your work will directly protect patient safety and trial integrity on a global scale.
- You'll turn data into decisions - using clinical data analytics and performance monitoring systems to spot trends, surface insights, and equip senior leaders with the evidence they need to act with confidence.
- You'll influence without authority - partnering across R&D Quality, Global Drug Development Operations, Regional Clinical Compliance, and beyond.
Your ability to connect, align, and inspire cross-functional teams will be your greatest tool.
- You'll think globally, act locally - managing risk across processes, programmes, studies, regions, countries, suppliers, sites, and investigators.
You'll ensure the right risks reach the right people at the right time.
- You'll build a culture people feel proud of - championing Quality Excellence and Inspection Readiness not as a mandate, but as a mindset.
You'll coach colleagues, mentor new team members, and make risk management feel like a business enabler, not a burden.
What's in it for you?
- Real impact, real visibility.
You'll sit within BMS's broader Risk Governance structure, giving you direct exposure to senior leadership and strategic decision-making.
Your recommendations won't disappear into a committee - they'll shape how clinical operations run globally.
- A seat at the table for innovation.
You'll lead risk-based innovation and education efforts.
If you have ideas about how clinical risk management should evolve, this is a place where those ideas are welcomed and acted upon.
- Career growth baked in.
With 8+ years of experience, you're ready to lead and this role stretches you further.
You'll manage complex, multi-layered projects, drive continuous improvement initiatives, and develop the skills that open doors at the highest levels of clinical development.
- A team that actually collaborates.
Cross-functional, global, matrixed - yes, it sounds complex, but it means you'll never work in a silo.
You'll build relationships across geographies and disciplines, growing a professional network that lasts a career.
- The BMS difference.
We're a company that genuinely believes in putting patients first.
When you're doing this work here, every risk you mitigate, every process you improve, and every team you empower connects back to a patient who needs a therapy to work.
- You're likely a great fit if…
- You have 8+ years in clinical trial operations and/or GCP compliance and you're known as a go-to expert in risk management within your organisation.
- You're comfortable in complexity - navigating global matrices, managing multiple priorities, and keeping your cool when stakes are high.
- You can walk into a room of mixed audiences - from scientists to senior executives - and communicate risk in a way that lands and drives action.
- You lead through influence, not hierarchy, and you take genuine pride in helping others grow.
- You're data-fluent you love a good trend, know how to visualise insights, and can translate numbers into narratives that move people.
- You hold a Bachelor's degree (life sciences preferred) and an advanced degree? Even better.
- Occasional travel required - because some of the best conversations still happen in person.
We hire for skills and capabilities, not just credentials – if this role excites you, but doesn't perfectly match your resume, we encourage you to apply anyway.
How We Work
Where you work matters – because collaboration, innovation and patient impact happen in many settings.
Our roles are structured across four work models site-essential, site-by-design, field-based and remote-by-design.
The model assigned to this role is based on its core responsibilities.
Learn more at https //careers. bms. com/ways-of-working.
Supporting People With Disabilities
BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles.
Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer.
If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to adastaffingsupport@bms. com.
Visit careers. bms. com/eeo-accessibility to access our complete Equal Employment Opportunity statement.
- Bristol Myers Squibb is Disability Confident – Employer
- A UK Government scheme
- Candidate Rights
BMS will consider qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.
For roles based in Los Angeles County only If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information https //careers. bms. com/california-residents/
Data Protection
We will never request payments, financial information, or social security numbers during our application or recruitment process.
Learn more about protecting yourself at https //careers. bms. com/fraud-protection.
Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.
If this posting is missing required information required by local law or incorrect, contact BMS at TAEnablement@bms. com with the Job Title and Requisition number.
Do not send application-related inquiries to this email.
To check your application status, please login to your Candidate Home Account.
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Associate Director, Business Risk Lead (EU) in Denham employer: Bristol Myers Squibb
At Bristol Myers Squibb, we offer a unique opportunity for Integrated Healthcare Managers to engage in meaningful work that truly transforms lives. Our supportive culture fosters professional growth and innovation, while our competitive benefits ensure a healthy work-life balance. Join us in the South UK, where you can thrive in a dynamic environment alongside passionate colleagues dedicated to making a real difference in the field of haematology-oncology.
StudySmarter Expert Advice🤫
We think this is how you could land Associate Director, Business Risk Lead (EU) in Denham
✨Unlock Networking Opportunities
Dive into industry-specific events like pharmaceutical conferences and seminars, where you can meet hiring managers from companies like Bristol Myers Squibb. These are goldmines for making connections and learning about job openings before they hit the mainstream job boards.
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Get involved with organisations such as the Royal Pharmaceutical Society or your local pharmaceutical professionals' network. Being an active member can boost your credibility and may even lead to job referrals in top organisations like Bristol Myers Squibb.
✨Leverage Internships for Full-time Roles
If you can, consider pursuing internships in the pharmaceutical industry, especially with companies like Bristol Myers Squibb. These opportunities often pave the way for full-time positions and allow you to demonstrate your capabilities firsthand.
✨Tailor Your Approach
When you're applying for roles, don't rush it! Take the time to customise your applications for specific positions, showcasing relevant skills and experiences that align with what Bristol Myers Squibb is looking for. A tailored application can really make you stand out!
We think you need these skills to ace Associate Director, Business Risk Lead (EU) in Denham
Some tips for your application 🫡
Showcase Your Relevant Experience:When applying for a role in the pharmaceutical industry, it's crucial to highlight any relevant experience you have. Whether that's internships, lab work, or even related coursework, make sure to weave this into your CV and cover letter. We want to see how your background aligns with the role you're applying for at Bristol Myers Squibb!
Emphasise Your Understanding of Regulations:The pharmaceutical industry is heavily regulated, so it's important to indicate your familiarity with industry standards and regulations. In your cover letter, mention any training or certifications you've received that are relevant, or discuss projects where you’ve navigated compliance. This will show Bristol Myers Squibb that you're not just a fit for the job but also a safety-conscious candidate!
Tailor Your CV to Be Result-Driven:Craft your CV to highlight quantifiable achievements, especially if you have previous roles in pharmaceuticals or related fields. Use metrics to demonstrate your impact, such as improved processing times or successful project completions while working on trials. This analytical approach will resonate well with hiring managers at Bristol Myers Squibb!
Convey Your Passion for the Industry:In your cover letter, express why you are passionate about working in the pharmaceutical sector. Whether it’s your desire to contribute to groundbreaking drug research or improve patient outcomes, let it shine through! At Bristol Myers Squibb, we value candidates who are truly enthusiastic about their work—you might just stand out from the crowd.
How to prepare for a job interview at Bristol Myers Squibb
✨Understand the Science
Make sure you brush up on key pharmaceutical concepts and recent developments in the industry. You might get asked some technical questions during the interview at Bristol Myers Squibb that show your grasp of drug development processes or regulatory requirements, so be ready to discuss them clearly.
✨Showcase Relevant Experience
If you have any hands-on experience or internships in a laboratory setting, be sure to highlight these in your responses. Think about the projects you worked on, the methodologies you used, and the impact you made. It's all about telling a story that connects your background to the role you're applying for.
✨Know Their Products
Take some time to familiarise yourself with Bristol Myers Squibb’s product range and recent breakthroughs. Understanding their portfolio not only shows your enthusiasm for the role but also allows you to ask insightful questions that demonstrate your interest in actively contributing to their projects.
✨Be Ready for Regulatory Scenarios
In a full-time pharmaceutical role, understanding the regulatory landscape is crucial. Prepare for situational questions that may test your problem-solving skills concerning compliance and safety standards. You could be asked how you'd handle a hypothetical issue regarding a drug’s market release, so think through your approach.