Senior Clinical SAS Programmer & Data Standards Lead
Senior Clinical SAS Programmer & Data Standards Lead

Senior Clinical SAS Programmer & Data Standards Lead

Full-Time 54000 - 84000 £ / year (est.) No home office possible
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At a Glance

  • Tasks: Lead the creation of ADaM datasets and develop SAS programming for clinical trials.
  • Company: Global clinical data analytics company based in Greater London.
  • Benefits: Competitive salary, career advancement, and a collaborative work environment.
  • Why this job: Elevate your career in clinical research and make a significant impact.
  • Qualifications: 8+ years of experience in SAS programming, with 2+ years in a lead role.
  • Other info: Join a dynamic team and contribute to innovative clinical data solutions.

The predicted salary is between 54000 - 84000 £ per year.

A global clinical data analytics company based in the Greater London area is seeking a seasoned professional to oversee the creation of ADaM datasets and develop SAS programming for clinical trials. The ideal candidate has 8+ years of experience, with at least 2 years in a lead role.

Responsibilities include:

  • Managing SAS code
  • Ensuring regulatory compliance
  • Collaborating with cross-functional teams

This role represents an excellent opportunity to further your career in clinical research and data analysis.

Senior Clinical SAS Programmer & Data Standards Lead employer: Cytel Inc

Join a leading global clinical data analytics company in the vibrant Greater London area, where you will thrive in a collaborative and innovative work culture. We offer competitive benefits, a commitment to employee growth through continuous training and development, and the chance to make a meaningful impact in the field of clinical research. With a focus on regulatory compliance and teamwork, this role provides an exceptional opportunity for seasoned professionals to advance their careers while contributing to groundbreaking projects.
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Contact Detail:

Cytel Inc Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land Senior Clinical SAS Programmer & Data Standards Lead

✨Tip Number 1

Network like a pro! Reach out to your connections in the clinical data field and let them know you're on the lookout for opportunities. You never know who might have a lead on a Senior Clinical SAS Programmer role!

✨Tip Number 2

Prepare for those interviews! Brush up on your SAS programming skills and be ready to discuss your experience with ADaM datasets. We want you to showcase your expertise and how you've led teams in the past.

✨Tip Number 3

Don’t forget to tailor your approach! When applying through our website, highlight your leadership experience and regulatory compliance knowledge. Make it clear why you’re the perfect fit for the role.

✨Tip Number 4

Follow up after interviews! A quick thank-you email can go a long way in keeping you top of mind. Remind them of your passion for clinical research and data analysis, and how you can contribute to their team.

We think you need these skills to ace Senior Clinical SAS Programmer & Data Standards Lead

SAS Programming
ADaM Dataset Creation
Regulatory Compliance
Clinical Trials Management
Cross-Functional Collaboration
Data Analysis
Leadership Skills
Project Management
Attention to Detail
Problem-Solving Skills
Experience in Clinical Research
Communication Skills

Some tips for your application 🫡

Tailor Your CV: Make sure your CV highlights your 8+ years of experience and any leadership roles you've held. We want to see how your background aligns with the responsibilities mentioned in the job description, especially around ADaM datasets and SAS programming.

Showcase Your Skills: In your cover letter, emphasise your expertise in managing SAS code and ensuring regulatory compliance. We love seeing specific examples of how you've collaborated with cross-functional teams in your previous roles.

Be Clear and Concise: When writing your application, keep it straightforward and to the point. We appreciate clarity, so avoid jargon and make sure your passion for clinical research and data analysis shines through.

Apply Through Our Website: We encourage you to submit your application directly through our website. It’s the best way for us to receive your details and ensures you’re considered for this exciting opportunity!

How to prepare for a job interview at Cytel Inc

✨Know Your SAS Inside Out

Make sure you brush up on your SAS programming skills, especially around ADaM datasets. Be prepared to discuss specific projects where you've used SAS in clinical trials, and how you ensured regulatory compliance.

✨Showcase Your Leadership Experience

Since the role requires at least 2 years in a lead position, be ready to share examples of how you've successfully managed teams or projects. Highlight your ability to collaborate with cross-functional teams and how you’ve driven results.

✨Understand the Company’s Mission

Research the company’s goals and values. Being able to articulate how your experience aligns with their mission will show that you’re genuinely interested in the role and can contribute positively to their objectives.

✨Prepare Questions for Them

Have a few thoughtful questions ready to ask at the end of the interview. This could be about their data standards or how they approach regulatory compliance. It shows you're engaged and have done your homework!

Senior Clinical SAS Programmer & Data Standards Lead
Cytel Inc
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  • Senior Clinical SAS Programmer & Data Standards Lead

    Full-Time
    54000 - 84000 £ / year (est.)
  • C

    Cytel Inc

    200-500
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