Senior SDTM Programmer β€” Technical Lead (Hybrid) in Denham

Senior SDTM Programmer β€” Technical Lead (Hybrid) in Denham

Denham Full-Time 63000 - 77000 Β£ / year (est.) Hybrid
Bristol-Myers Squibb Co

At a Glance

  • Tasks: Lead SDTM programming for pivotal studies and global regulatory submissions.
  • Company: Join Bristol Myers Squibb, a leader in the pharmaceutical industry.
  • Benefits: Hybrid work model, competitive salary, and opportunities for mentorship.
  • Other info: Mentor junior programmers and collaborate with CROs in a dynamic environment.
  • Why this job: Shape SDTM strategies and make a real impact in healthcare.
  • Qualifications: 4+ years in pharma/CRO with deep CDISC/SDTM expertise and strong SAS skills.

The predicted salary is between 63000 - 77000 Β£ per year.

Bristol Myers Squibb is seeking a Senior SDTM Statistical Programmer to lead SDTM programming for pivotal studies and global regulatory submissions.

You will be the technical lead on assigned studies, shaping SDTM strategies from protocol review through to submission, and you will mentor junior programmers and collaborate with CROs.

The role requires 4+ years in pharma/CRO, deep CDISC/SDTM expertise, and strong SAS skills across complex data environments.

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Senior SDTM Programmer β€” Technical Lead (Hybrid) in Denham employer: Bristol-Myers Squibb Co

Bristol Myers Squibb is an exceptional employer, offering a dynamic work culture that fosters collaboration and innovation. As a Strategic Country Controller for Switzerland & Austria, you will benefit from extensive professional growth opportunities while working in a supportive environment that values integrity and excellence. With the chance to engage with global finance teams and contribute to impactful financial strategies, this role provides a meaningful career path in a leading biopharmaceutical company.

Bristol-Myers Squibb Co

Contact Details:

Bristol-Myers Squibb Co Recruitment Team

StudySmarter Expert Advice🀫

We think this is how you could land Senior SDTM Programmer β€” Technical Lead (Hybrid) in Denham

✨Unlock Networking Opportunities

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✨Join Relevant Professional Bodies

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 Co.

✨Leverage Internships for Full-time Roles

If you can, consider pursuing internships in the pharmaceutical industry, especially with companies like Bristol-Myers Squibb Co. 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 Co is looking for. A tailored application can really make you stand out!

We think you need these skills to ace Senior SDTM Programmer β€” Technical Lead (Hybrid) in Denham

SDTM Programming
CDISC Expertise
SAS Skills
Technical Leadership
Mentoring
Collaboration with CROs
Protocol Review

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 Co!

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 Co 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 Co!

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 Co, we value candidates who are truly enthusiastic about their workβ€”you might just stand out from the crowd.

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

✨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 Co 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 Co’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.