Company:
Katalyst Healthcares & Life Sciences
Location: Bridgewater
Closing Date: 20/10/2024
Hours: Full Time
Type: Permanent
Job Requirements / Description
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.
Requirements:
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.
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.
Requirements:
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.