Full Time

Senior SAS Programmer – United Kingdom

Posted 1 month ago
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Job Description

Job Summary:

We are seeking a talented Senior SAS Programmer to join our team. The successful candidate will be responsible for developing and validating SAS programs in support of clinical trials and other research projects. As a Senior SAS Programmer, you will be responsible for leading and mentoring junior programmers, as well as collaborating with cross-functional teams to ensure high-quality deliverables.

About the Company:

Our company is a global provider of clinical research services and solutions to pharmaceutical, biotechnology, and medical device companies. We specialize in helping our clients bring innovative therapies to patients faster, and our team of experienced professionals is dedicated to delivering high-quality results in a timely and cost-effective manner.

Our culture is one of collaboration, innovation, and a commitment to excellence. We value our employees and invest in their growth and development, providing opportunities for training, career advancement, and work-life balance. Our state-of-the-art facilities and cutting-edge technology enable us to stay at the forefront of the industry, and our commitment to quality and compliance ensures that we deliver the best possible outcomes for our clients.

Responsibilities:

  • Developing and validating complex SAS programs for clinical trials and other research projects, ensuring high-quality and timely deliverables.
  • Leading and mentoring a team of SAS programmers, providing guidance and support to help them grow and develop their skills.
  • Collaborating with cross-functional teams, including statisticians, data managers, and medical writers, to ensure that data is accurate, consistent, and reliable.
  • Participating in project planning, providing input on timelines, resource needs, and potential issues related to programming tasks.
  • Contributing to the development and implementation of programming standards and best practices, ensuring adherence to regulatory guidelines and industry standards.
  • Reviewing and providing feedback on study protocols, statistical analysis plans, and other project-related documentation.
  • Conducting quality control checks on programming outputs, identifying and resolving discrepancies and errors.
  • Staying up-to-date with emerging trends and technologies in SAS programming, and sharing knowledge and expertise with colleagues.
  • Providing support for regulatory submissions and audits, as needed.

Qualifications:

  • Bachelor’s degree in computer science, statistics, or related field; Master’s degree preferred
  • Minimum of 5 years of experience in SAS programming for clinical trials or related research
  • Experience leading and mentoring junior programmers
  • Strong knowledge of SAS programming language and SAS macros
  • Excellent analytical and problem-solving skills
  • Strong communication and interpersonal skills, with the ability to work effectively in a team environment

If you are a motivated, self-directed individual with a passion for programming and a desire to make a difference in the lives of patients, we encourage you to apply for this exciting opportunity. We offer a competitive salary and benefits package, as well as a dynamic and rewarding work environment.

If this job doesn’t quite interest you, we may have other opportunities that are more relevant.

So please visit our website – www.glshub.com or reach out via:

Tel – +44 (0) 204 599 8130

Email – christopher@glshub.com