Fortrea is seeking an Associate Programmer II to support clinical operations by assisting in the design, development, and maintenance of clinical databases and SAS programming. This role is critical in ensuring compliance with CDISC standards, EDC systems (Medidata Rave, Inform), and clinical data reporting.
Key Responsibilities:
✔ Design, develop, and maintain clinical EDC databases (Rave, Inform, etc.)
✔ Develop SAS programs for data extraction, transformation, and loading (ETL)
✔ Ensure adherence to Fortrea SOPs, CDISC standards, and Good Clinical Practices (GCP)
✔ Collaborate with cross-functional teams to deliver high-quality clinical data solutions
✔ Troubleshoot and resolve technical issues related to clinical data systems
✔ Continuously improve technical and problem-solving skills
Qualifications & Experience:
✅ Education: Degree in Life Sciences, IT, or related field (or certification in allied health)
✅ Experience: 0-2 years in EDC programming, SAS programming, or clinical data management
✅ Technical Skills: Knowledge of Medidata Rave, Inform, SAS, or other EDC tools
✅ Soft Skills: Strong problem-solving, communication, and teamwork abilities
✅ Preferred: Understanding of clinical trial processes, CDISC standards, and biometrics
About Fortrea
Fortrea is a leading global contract research organization (CRO) dedicated to providing biopharmaceutical, medical device, and diagnostic companies with comprehensive clinical development solutions. With a focus on innovation and compliance, Fortrea plays a crucial role in advancing clinical research and drug development.
Why Join Fortrea?
✔ Work on cutting-edge clinical trials with global impact
✔ Collaborative and supportive work environment
✔ Opportunities for career growth and skill development
