Company:
Katalyst Healthcares & Life Sciences
Location: Chicago
Closing Date: 19/11/2024
Hours: Full Time
Type: Permanent
Job Requirements / Description
Responsibilities:
Responsible for supporting the Programming deliveries of a clinical study or project.
Implements statistical programming aspects of the protocol and the clinical development program
Ensures high quality is built into own deliverables and the quality delivered by other programmers
Programs independently with high efficiency and quality
Writes and/or implements specifications and oversees completeness of relevant documentation
Contribute to the development of best practice to improve quality, efficiency and effectiveness within function
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
Works proactively with study team members including but not limited to the Statistician, Lead Programmer, Data Manager and Study Leader.
Requirements:
Bachelor's degree in computer science (CS), statistics or related scientific disciplines with 7 yrs. clinical programming (CDISC) experience; Master's degree in CS, statistics or related disciplines with 5 yrs. of clinical programming (CDISC) experience.
Require strong Oncology TA with experience in ISS & Client.
Experience in blood cancer and the Lugano criteria is a plus.
Excellent programming skills including macro language.
Ability to proactively manage concurrent activities within a study or part of project.
Proficient knowledge of the clinical development process.
Responsibilities:
Responsible for supporting the Programming deliveries of a clinical study or project.
Implements statistical programming aspects of the protocol and the clinical development program
Ensures high quality is built into own deliverables and the quality delivered by other programmers
Programs independently with high efficiency and quality
Writes and/or implements specifications and oversees completeness of relevant documentation
Contribute to the development of best practice to improve quality, efficiency and effectiveness within function
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
Works proactively with study team members including but not limited to the Statistician, Lead Programmer, Data Manager and Study Leader.
Requirements:
Bachelor's degree in computer science (CS), statistics or related scientific disciplines with 7 yrs. clinical programming (CDISC) experience; Master's degree in CS, statistics or related disciplines with 5 yrs. of clinical programming (CDISC) experience.
Require strong Oncology TA with experience in ISS & Client.
Experience in blood cancer and the Lugano criteria is a plus.
Excellent programming skills including macro language.
Ability to proactively manage concurrent activities within a study or part of project.
Proficient knowledge of the clinical development process.
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