Our dedicated Statistical Programmers in our Clinical Development Services (CDS) and Clinical Pharmaceutical Services (CPS) business units are central to the successful delivery of complex clinical trials for renowned, innovative and global top pharmaceutical and biotech companies. Based in our Leeds office, these teams are constantly growing and are now looking for new teammates keen on commencing their programming career in clinical research.

This entry level position allows you to participate in the development of innovative new benchmark drugs for a wide variety of therapeutic areas such as oncology, cardiovascular, respiratory, neurological, diabetes, rare diseases, pain, immunology etc. Your expertise and your work as a statistical programmer has a direct impact on improving the health and lives of thousands of patients around the globe every day. Join us and see why more than 90% of the top 20 global pharmaceutical companies are repeat customers!

What else can you expect from us?

• Rewarding and meaningful work in an established, diverse, highly profitable and respected global company

• Highly competitive compensation packages, including various local benefits such as pension contributions, complimentary health insurance plans, remote working allowances etc.

• A genuine work life balance

• Flexibility in working hours

• A thorough onboarding with support from your personal mentor

• A permanent employment contract with Labcorp Drug Development

• Excellent training and career development opportunities, as well as support with advancing your individual education

• Strong support from your Line Manager and your team, as well as from more than 20,000 colleagues worldwide

Your responsibilities:

• Develop and maintain programs using SAS to create CDSIC SDTM and ADaM datasets as well as Tables, Figures and Listings (TFLs)

• Following department guidelines perform self-checks of code and outputs to ensure first time quality

• Effective time management in order to meet delivery deadlines

• Communicate accurate and timely status updates to line manager, lead programmer, and other associates

• Conduct all activities according to the defined project-specific quality and performance standards as well as relevant SOPs, international guidelines for clinical trials such as ICH/GCP, and local requirements

• Actively contribute to the success of relevant project activities and administrative/departmental initiatives

Your profile:

• Degree in a relevant field such as mathematics, life sciences, (bio-)statistics, computer sciences, etc.

• In lieu of the above: an equivalent completed vocational training and / or equivalent professional experience in programming

• Ideally, an interest in life sciences, particularly medicine, biology and drug development

• Strong organizational and communication skills

• Ability to learn new systems and flourish in an evolving technical environment

• A collaborative work style, good problem solving abilities. and a keen attention to detail

• Business fluency in English – both verbal and written – is a must

As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff conducting operations in more than 90 countries, Fortrea is transforming drug and device development for partners and patients across the globe.

Did you know?

Labcorp's Clinical Development and Commercialization Services business is now Fortrea in connection with its planned spin-off from Labcorp, which is expected in mid-2023. Fortrea’s spin-off from Labcorp is subject to satisfaction of certain customary conditions. This spin-off will position both organizations for accelerated growth and allow each to focus resources on distinct strategic priorities, customer and employee needs and value creation opportunities. As a provider of phase I-IV clinical trial management, regulatory guidance, patient access solutions and market access consulting, Fortrea will partner with both emerging and large pharmaceutical, biotechnology, device and diagnostic companies to drive healthcare innovation and improve the lives of patients worldwide.

Fortrea is looking for problem-solvers and creative thinkers who are passionate about breaking down barriers faced by sponsors of clinical trials, and who are committed to helping transform the development process to get promising life-changing ideas and therapies to patients faster. Join us as we cultivate a workspace where all employees have the opportunity to grow and make impacts on a global scale. For more information and questions related to Fortrea, please visit www.fortrea.com.

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