Lead Clinical SAS Programmer

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November 5

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Fortrea

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Biotechnology • Pharmaceuticals • Healthcare Insurance

Fortrea is a global clinical research organization (CRO) specializing in providing comprehensive clinical development services to biopharma and MedTech companies. With over 30 years of experience, Fortrea offers a range of services including clinical pharmacology, phase I-IV study management, regulatory strategy, market access, and more. They focus on advancing healthcare innovation by integrating data and scientific expertise to deliver tailored solutions that enable faster decision-making and improve patient outcomes, especially in the realm of cell and gene therapy programs, as well as various therapeutic areas like oncology, cardiovascular, and infectious diseases.

10,000+ employees

🧬 Biotechnology

💊 Pharmaceuticals

⚕️ Healthcare Insurance

📋 Description

• Assist with leading EDC Builds and mentor the study team in SAS or other proprietary software • Lead the development of visual analytics dashboard using tools like Spotfire/Tableau • Functions as Subject Matter Expert (SME) and Lead on multiple projects • Co-ordinate activities of all programmers across projects and provide technical/functional expertise • Develop/validate Custom/Complex Edit-Check programs, reports, and efficiently handle external data and data reconciliations • Plan, execute and oversee all programming activities on a study • Meet with Data Manager on assigned projects to discuss technical strategies, contractual obligations, and timelines • Conduct team meetings, provides technical guidance/assistance to Programmers, and perform other duties as assigned by Manager

🎯 Requirements

• Bachelor's degree (life sciences, health sciences, information technology or related subjects preferred) • 7 to 9 years of relevant work experience to include data management programming activities including SAS Programming • Demonstrated skill in leading teams, by example and mentoring staff • Excellent oral and written communication and presentation skills • Knowledge of clinical trial process and data management, CRF design, and systems applications • Working knowledge of the relationship and regulatory obligation of the CRO industry with pharmaceutical/biotechnological companies • Demonstrated ability to handle multiple competing priorities

🏖️ Benefits

• Highly competitive compensation packages • Various local benefits such as pension contributions • Complimentary health insurance plans • Remote working allowances • A genuine work life balance • Flexibility in working hours • A thorough onboarding with support from your personal mentor • A permanent employment contract with Fortrea and a rewarding career progression