Associate Director, Clinical Data Management in Denham

Associate Director, Clinical Data Management in Denham

Denham Full-Time 80000 - 100000 £ / year (est.) Home office (partial)
Bristol-Myers Squibb Company

At a Glance

  • Tasks: Lead clinical data management to drive life-changing medicines from lab to patients.
  • Company: Join a leading biopharma company making a real impact in healthcare.
  • Benefits: Competitive salary, career growth, and opportunities to mentor future talent.
  • Other info: Dynamic role with travel opportunities and a commitment to diversity.
  • Why this job: Shape the future of clinical trials and influence global health outcomes.
  • Qualifications: 7+ years in biopharma with strong leadership and data management skills.

The predicted salary is between 80000 - 100000 £ per year.

We're looking for an Associate Director of Clinical Data Management to join us at our Uxbridge site. This is a role where your expertise doesn't just support a clinical trial – it drives it. The data you champion, the standards you set, and the teams you lead are what ultimately move life‑changing medicines from the lab to the people who need them most. In this position you will lead cross‑functional teams, represent data management at the executive level, and set the standard that others follow. You won’t be working in isolation – you will drive the program from strategy through to regulatory submission.

Responsibilities

  • Own end‑to‑end data management across one or more complex, high‑stakes clinical development programmes with autonomy to shape processes.
  • Set programme‑level data standards in partnership with global teams, creating a lasting legacy beyond any single trial.
  • Lead Data Quality Review meetings to ensure integrity and completeness of trial data that underpins regulatory submissions worldwide.
  • Mentor junior Data Management Leads and build the next generation of talent while advancing your own leadership reputation.
  • Represent Data Management on cross‑functional and regulatory submission teams, providing visibility and influence across the organization.
  • Oversee EDC systems (Medidata RAVE), integrate data from eCOA, external data, and Safety Gateway platforms, and manage third‑party vendors and CROs to ensure SLA compliance.
  • Author and review critical study documentation – from Data Quality Management Plans to eCRF Completion Guidelines.
  • Lead or support Health Authority inspections and audits when they occur.
  • Travel 5–10% to industry conferences, investigator meetings, and regulatory inspections.

Qualifications

  • 7+ years of experience in biopharma or CRO environments, with at least 3 years in a study or program leadership role.
  • Strong working knowledge of FDA/ICH guidelines and industry data management practices.
  • Hands‑on experience with EDC systems, ideally Medidata RAVE.
  • Sharp eye for metrics, reporting, and quality oversight.
  • Excellent communication skills to hold a room – from junior team members to senior regulatory authorities.
  • Bachelor’s degree in life sciences, data science, or statistics (an advanced degree is a bonus, not a barrier).

We are committed to equal employment opportunity and do not discriminate on the basis of race, colour, religion, sex, national origin, disability, or any other protected class.

Associate Director, Clinical Data Management in Denham employer: Bristol-Myers Squibb Company

At our Uxbridge site, we pride ourselves on being an exceptional employer that fosters a collaborative and innovative work culture. As an Associate Director of Clinical Data Management, you will not only lead critical projects that impact patient lives but also benefit from extensive professional development opportunities and mentorship programmes designed to enhance your leadership skills. Join us to be part of a mission-driven team where your contributions are valued, and you can make a real difference in the biopharma industry.

Bristol-Myers Squibb Company

Contact Details:

Bristol-Myers Squibb Company Recruitment Team

StudySmarter Expert Advice🤫

We think this is how you could land Associate Director, Clinical Data Management in Denham

Get Involved in Local Research Communities

Tap into local biotechnology meetups and research forums. These are great places to mingle with industry professionals, share your passion, and even discover unadvertised job openings. It's all about getting your face known in the field!

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Show Off Your Projects

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Stay Up-to-Date with Industry Trends

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We think you need these skills to ace Associate Director, Clinical Data Management in Denham

Clinical Data Management
Cross-Functional Team Leadership
Data Quality Review
Regulatory Submission
EDC Systems (Medidata RAVE)
Data Standards Development
Mentoring and Talent Development

Some tips for your application 🫡

Show Off Your Lab Skills:In the biotechnology field, it's super important to highlight your lab experience in your CV. Be sure to mention specific techniques or instruments you've mastered (think PCR, gel electrophoresis, etc.) and any relevant projects you've worked on. This will show Bristol-Myers Squibb Company that you have the hands-on skills they need.

Tailor Your Technical Skills:Make sure to emphasise your technical skills, especially those relevant to the biotechnology sector. Include any software tools or programming languages you've used, like R or Python for data analysis, which could be key for this role at Bristol-Myers Squibb Company.

Craft a Compelling Cover Letter:Since this is a full-time role, your cover letter should reflect not only your passion for biotechnology but also your long-term career ambitions. Share why you're excited about the work that Bristol-Myers Squibb Company does and how you envision contributing to their goals. This shows that you’re not just looking for any job, but you're genuinely invested in this opportunity.

Include Your Papers and Projects:If you've published any papers or contributed to significant projects, mention them! These documents can boost your application and provide tangible evidence of your expertise in the biotechnology field. Don’t forget to link to any relevant publications or project summaries—this can set you apart from other candidates.

How to prepare for a job interview at Bristol-Myers Squibb Company

Brush Up on Lab Techniques

Since you're eyeing a full-time gig in biotechnology, make sure you're well-versed in the lab techniques relevant to the role. Be ready to talk about PCR, CRISPR, or any specific methods mentioned in the job description at Bristol-Myers Squibb Company. You might even be asked to demonstrate your understanding of these processes.

Know Your Bioinformatics Tools

Get comfortable with bioinformatics tools that are commonly used in the industry, like BLAST or Bioconductor. These are key in biotechnology, and having hands-on experience or at least familiarity can set you apart. Prepare to discuss any relevant projects you've worked on, especially if they involved data analysis or genomic research.

Show Your Teamwork Skills

Biotech often involves collaboration across multiple disciplines. Be ready to share stories that highlight your teamwork and communication skills, especially in research projects. Think about working with different teams at university or any internships – this is where you can show how well you fit into Bristol-Myers Squibb Company's culture.

Research Recent Biotech Innovations

Stay updated on the latest trends and breakthroughs in biotechnology. Knowing what's happening in the field can help you engage in more meaningful discussions during your interview. Bring up recent articles or advancements that excite you, especially those related to the work being done at Bristol-Myers Squibb Company. This shows your passion for the industry!