Senior Statistical Programmer – SAS & Clinical Trials Lead in Reading

Senior Statistical Programmer – SAS & Clinical Trials Lead in Reading

Reading Full-Time 63000 - 77000 Β£ / year (est.) No working from home possible
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At a Glance

  • Tasks: Analyse clinical trial data and lead statistical programming tasks.
  • Company: ICON plc, a top healthcare intelligence and clinical research organisation.
  • Benefits: Competitive salary, career development, and a supportive work environment.
  • Other info: Opportunity to mentor others and grow in a dynamic field.
  • Why this job: Make a real impact in healthcare by ensuring high-quality results.
  • Qualifications: Experience in statistical programming and strong collaboration skills.

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

ICON plc, a leading healthcare intelligence and clinical research organization, is seeking a Senior Statistical Programmer I in Reading.

You will analyse clinical trial data and support the statistical analysis process to ensure high-quality results.

You will lead on statistical programming tasks with depth, collaborating with biostatisticians, and contributing to regulatory submissions.

The role emphasizes quality, independence, and mentoring others as needed.

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Senior Statistical Programmer – SAS & Clinical Trials Lead in Reading employer: JobsInSAS.com

ICON plc is an exceptional employer that fosters a collaborative and innovative work culture in Reading, where employees are empowered to lead and mentor within the realm of clinical trials. With a strong emphasis on professional growth, ICON offers extensive training and development opportunities, ensuring that team members can thrive in their careers while contributing to impactful healthcare solutions. The company's commitment to quality and independence makes it a rewarding place for those looking to make a meaningful difference in the field of clinical research.

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Contact Details:

JobsInSAS.com Recruitment Team

We think you need these skills to ace Senior Statistical Programmer – SAS & Clinical Trials Lead in Reading

Statistical Programming
SAS
Clinical Trial Data Analysis
Collaboration with Biostatisticians
Regulatory Submissions
Quality Assurance
Independence