Offer summary

Qualifications:

5+ years of programming experience in a relevant field., Bachelor's and/or Master's Degree in Computer Science, Engineering, Mathematics, or Statistics., Experience in SAS programming and knowledge of relational database structures., Excellent communication and interpersonal skills, with SAS certification preferred..

Key responsabilities:

Implement and execute programming and project standards for clinical studies.

Support requests for statistical and non-statistical analyses and maintain documentation.

Apply standard tools and participate in the development of new programming standards.

Adhere to company SOPs and guidelines while performing other duties as needed.

Katalyst Healthcare's & Life Sciences (Katalyst HLS) is a Global Contract Research Organisation that provides End-to-End Clinical Research Services for Healthcare and Life Sciences companies globally. At Katalyst HLS offers ICH-GCP compliant clinical trial services from Phase I–IV in all key therapeutic areas to support clinical development and research requirements and also provides validation, quality and regulatory services for Pharma/Bio-Pharma/Medical Device industries. Services:- Clinical Trial Management- Clinical Data Management- Biostatistics & Statistical Programming- Medical Writing- Pharmacovigilance- Quality and Regulatory Affairs- GMP, GLP and GCP Validations- Manufacturing Process Validations- Equipments & Instruments Validations- Computer Systems Validations- Human Resourcing

Job description

Responsibilities:

Implement and execute the programming and project standards
Support ongoing clinical studies requests for statistical and non-statistical analyses
Provide documentation and consistent maintenance of code, logs, and output in a regulated environment
Apply standard tools developed for the study or project; participate in development of new standards and tools.
Follow all company SOP and guidelines in the creation of the programming deliverables
Adheres to procedures surrounding retention of data, records, and information for clinical studies
Perform other duties, as needed

Requirements:

5+ years of Programming experience
Bachelor's and/or Master's Degree in Computer Science, Engineering, Mathematics, and/or Statistics
Experience in SAS programming
Exposure of relational database structure
Solid understanding of reporting systems.
Experience with implementing standardization methodology
Great interpersonal skills
Excellent communication skills (written and verbal)
SAS certification
Programming experience in processing clinical trial data in the Biotechnology, Pharmaceutical, and/or Health-related industry