Lead Statistical Programmer - Clinical Trials & CDISC in London
Lead Statistical Programmer - Clinical Trials & CDISC

Lead Statistical Programmer - Clinical Trials & CDISC in London

London Full-Time 48000 - 72000 £ / year (est.) No home office possible
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At a Glance

  • Tasks: Lead statistical programming for clinical trials and manage CRO deliverables.
  • Company: Global pharmaceutical company focused on patient treatment innovation.
  • Benefits: Strong emphasis on training, development, and competitive salary.
  • Why this job: Join a team at the forefront of healthcare innovation and make a real difference.
  • Qualifications: Bachelor's degree and 7+ years in clinical development with SAS expertise.
  • Other info: Opportunity for career growth in a dynamic and supportive environment.

The predicted salary is between 48000 - 72000 £ per year.

A global pharmaceutical company is seeking a Principal Statistical Programmer to work embedded within a major client. The role focuses on delivering high-quality statistical programming, managing CRO deliverables, and ensuring adherence to FDA regulations.

Ideal candidates will have a Bachelor's degree and over 7 years of experience in clinical development, with excellent skills in SAS and communication. This is an opportunity to join a team at the forefront of patient treatment innovation, with a strong emphasis on training and development.

Lead Statistical Programmer - Clinical Trials & CDISC in London employer: Cytel

Join a leading global pharmaceutical company that prioritises innovation and excellence in patient treatment. With a strong commitment to employee development, you will benefit from extensive training opportunities and a collaborative work culture that values your contributions. Located in a dynamic environment, this role offers the chance to make a meaningful impact while working alongside industry experts.
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Contact Detail:

Cytel Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land Lead Statistical Programmer - Clinical Trials & CDISC in London

✨Tip Number 1

Network like a pro! Reach out to your connections in the pharmaceutical industry, especially those who work in clinical trials. A friendly chat can lead to insider info about job openings that might not even be advertised yet.

✨Tip Number 2

Prepare for interviews by brushing up on your SAS skills and understanding FDA regulations. We recommend doing mock interviews with friends or using online platforms to get comfortable discussing your experience and how it relates to the role.

✨Tip Number 3

Showcase your communication skills! During interviews, make sure to highlight how you've effectively managed CRO deliverables in the past. Use specific examples to demonstrate your ability to collaborate and lead teams.

✨Tip Number 4

Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, we’re always looking for passionate individuals who want to be at the forefront of patient treatment innovation.

We think you need these skills to ace Lead Statistical Programmer - Clinical Trials & CDISC in London

Statistical Programming
SAS
Clinical Development
CRO Management
FDA Regulations
Communication Skills
Training and Development
Attention to Detail
Problem-Solving Skills
Team Collaboration
Project Management
Data Analysis

Some tips for your application 🫡

Tailor Your CV: Make sure your CV highlights your experience in clinical development and your skills in SAS. We want to see how your background aligns with the role of Lead Statistical Programmer, so don’t be shy about showcasing relevant projects!

Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you’re passionate about statistical programming and how you can contribute to our mission in patient treatment innovation. Keep it concise but impactful!

Showcase Your Communication Skills: Since this role involves managing CRO deliverables, it’s crucial to demonstrate your communication prowess. We love candidates who can articulate complex ideas clearly, so include examples of how you've successfully collaborated with teams in the past.

Apply Through Our Website: We encourage you to apply directly through our website for a smoother application process. It helps us keep track of your application and ensures you don’t miss out on any important updates from us!

How to prepare for a job interview at Cytel

✨Know Your SAS Inside Out

Make sure you brush up on your SAS skills before the interview. Be prepared to discuss specific projects where you've used SAS in clinical programming, and think about how you can demonstrate your expertise in statistical analysis and data management.

✨Understand FDA Regulations

Since the role involves ensuring adherence to FDA regulations, it’s crucial to familiarise yourself with these guidelines. Be ready to talk about how you've navigated regulatory requirements in past roles and how you ensure compliance in your work.

✨Showcase Your Communication Skills

As a Lead Statistical Programmer, you'll need to manage CRO deliverables and collaborate with various teams. Prepare examples of how you've effectively communicated complex statistical concepts to non-technical stakeholders, highlighting your ability to bridge gaps between teams.

✨Emphasise Continuous Learning

This role is at the forefront of patient treatment innovation, so show your enthusiasm for ongoing training and development. Discuss any recent courses or certifications you've completed, and express your eagerness to stay updated with the latest trends in clinical trials and statistical programming.

Lead Statistical Programmer - Clinical Trials & CDISC in London
Cytel
Location: London
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  • Lead Statistical Programmer - Clinical Trials & CDISC in London

    London
    Full-Time
    48000 - 72000 £ / year (est.)
  • C

    Cytel

    100-200
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