Job
Description
As a SAS Clinical Programmer III at Allucent, a biopharmaceutical company focused on delivering life-changing therapies to patients worldwide, you will play a crucial role in supporting the analysis and reporting of clinical trial data. Your expertise in SAS programming and clinical data management will ensure the accuracy and integrity of our clinical databases. By leading and coordinating clinical programming activities, you will maintain databases in compliance with study-specific plans, standard operating procedures, and regulatory requirements. Your innovative approach will make a quick impact on our nimble global team. - Design, build, test, and release clinical databases, including study design specifications, User's Acceptance Test (UAT) test cases, and database configuration settings - Collaborate with SAS and EDC programming, review eCRF completion guidelines, develop/validate SAS programs for metric reporting, data review listings, and data import/export set-up - Apply CDISC conventions during database build activities and data warehousing - Review and adhere to study-specific data management documents/plans, actively participate in meetings, and use analytical problem-solving approaches - Maintain knowledge in clinical programming and data management by self-training, attending classes, proposing initiatives for efficiency, and contributing as a Subject Matter Expert (SME) Qualifications Required: - Minimum 2-5 years of relevant work experience in clinical research/drug development with a degree in Life Science, Computer Science, healthcare, or related field - Proficiency in SAS and EDC programming - Good knowledge of ICH-GCP(R2), GDPR/HIPPA, and applicable regulatory requirements - Strong understanding and hands-on experience with CDISC standards, programming languages such as PL/SQL, SAS, and comparable fields - Ability to work in a fast-paced challenging environment and collaborate effectively with team members,
