Clinical Data Programmer

Clinical Data Programmer

Have you got the desire to improve health and lives?

What you’ll be doing

Skills and Experience

• Bachelor’s Degree (B.S./B.A.); scientific discipline preferred. SAS certification may be considered in lieu of education requirement. • Significant experience with SAS; in a regulated environment or clinical research organization experience preferred • Demonstrated experience in SAS is required; including SAS macros, arrays, SQL, SAS Graph, and; knowledge with different output formats (e.g., .rtf, .xml, .xpt). • Proficiency with a programming language other than SAS (e.g., .NET, VBA) a plus. • Familiarity with the System Development Lifecycle (SDLC) a plus. • Demonstrated excellent organizational skills. • Basic familiarity with Microsoft Office Suite. • Computer skills, commensurate with Essential Functions, including the ability to learn a validated system. • Ability to work extended hours beyond normal work schedule to include, but not limited to evenings, weekends, extended shifts, and/or extra shifts, sometimes on short notice. • Ability to work under specific time constraints.
• All applicants must have full and permanent Right to Work in the UK as we are unable to provide sponsorship for this role.
• The salary range for this role is £30,000 - £34,000/annum + bonus + benefits. Please note that the salary varies within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.
• About Safety Assessment Charles River is committed to helping our partners expedite their preclinical drug development with exceptional safety assessment services, state-of-the-art facilities and expert regulatory guidance. From individual specialty toxicology and IND enabling studies to tailored packages and total laboratory support, our deeply experienced team can design and execute programs that anticipate challenges and avoid roadblocks for a smooth, efficient journey to market. Each year approximately 300 investigational new drug (IND) programs are conducted in our Safety Assessment facilities.
• About Charles River Charles River is an early-stage contract research organization (CRO). We have built upon our foundation of laboratory animal medicine and science to develop a diverse portfolio of discovery and safety assessment services, both Good Laboratory Practice (GLP) and non-GLP, to support clients from target identification through preclinical development. Charles River also provides a suite of products and services to support our clients’ clinical laboratory testing needs and manufacturing activities. Utilizing this broad portfolio of products and services enables our clients to create a more flexible drug development model, which reduces their costs, enhances their productivity and effectiveness to increase speed to market.
• With over 20,000 employees within 110 facilities in over 20 countries around the globe, we are strategically positioned to coordinate worldwide resources and apply multidisciplinary perspectives in resolving our client’s unique challenges. Our client base includes global pharmaceutical companies, biotechnology companies, government agencies and hospitals and academic institutions around the world.
• At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.
• At Charles River Laboratories, we recognize and recruit all talent. We are a company committed to fostering a sense of belonging and work daily in this direction.
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