Clinical SAS Programmer - Katalyst Healthcares & Life Sciences
Bridgewater, NJ 07920
About the Job
Responsibilities:
- Develop Tables, Figures, Listings (TFLs) deliverables from existing SAS programs for Clinical Study Report (CSR) if similar TFLs exist and from scratch for new outputs.
- Capacity for independent programming and review of reports and outputs.
- Customize outputs and graphics according to delivery specifications of target audience on the direction of biostatisticians.
- Responsible for supporting the Programming deliveries of a clinical study or project.
- Programs independently with high efficiency and quality.
- Ensures compliance with standards and automation usage.
- Plans and support team activities and tasks.
- Communicates and escalates risks within the assigned studies and/or projects.
- Bachelor's degree in computer science (CS), statistics, or related scientific disciplines with 4 yrs. of clinical programming (CDISC) experience.
- Master's degree in CS, statistics or related disciplines with 8 yrs. of clinical programming (CDISC) experience.
- Oncology/Hematology TA experience is required.
- ISS & Client experience is required.
- Working knowledge of ICH and Good Clinical Practices, Clinical research, Clinical trial process, and related regulatory requirements and terminology.
- Good understanding of the clinical drug development process.
- Strong communication skills and coordination skills.
Source : Katalyst Healthcares & Life Sciences
