Company:
Katalyst Healthcares & Life Sciences
Location: South Plainfield
Closing Date: 16/10/2024
Hours: Full Time
Type: Permanent
Job Requirements / Description
RESPONSIBILITIES:
Serve as the statistical programming lead on internal project teams and coordinate programming, verification, and documentation of statistical programs for use in creating analysis datasets, tables, listings, and figures.
Facilitate advanced technical expertise, in conjunction with internal and external team members, to design, implement, validate, and maintain project reporting applications that are supported by the department.
Assist in ensuring the optimum performance of group function.
May recommend and implement techniques to improve productivity, increase efficiencies, cut costs, take advantage of opportunities, and maintain state-of-the-art practices.
Work independently to carry out assignments with little direct supervision.
Identify project priorities and project timeline goals and communicate priority related issues and timelines to programming teams.
Ensure the efficiency, quality, and integrity of data reporting, and project activities executed.
Successfully represent the department and the company in sponsor meetings/presentations and maintain a positive working relationship with sponsors, collaborating associates, and vendor personnel.
Maintain awareness of project budgets and tasks, and effectively communicate the status of such tasks to line management and the project manager, as appropriate.
Perform other duties as required by the Department.
REQUIREMENTS:
I have an undergraduate degree or higher in Biostatistics, mathematics, Computer Science, or equivalent.
3 years of Statistical Programming/Statistics experience or an equivalent combination of education and experience to successfully perform the key responsibilities of the job.
3 years of one or more statistical software packages (SAS® preferred, and/or R and/or Python) used to conduct statistical analyses.
3 years working knowledge CDISC standards.
Previous experience in pharmaceutical research or CRO setting required.
Energized self-starter.
Excellent organizational skills.
Excellent communication skills, verbal and written.
Exceptional attention to detail.
Flexible, team player.
Proven ability to organize and effectively prioritize workload and deliverables.
Serve as the statistical programming lead on internal project teams and coordinate programming, verification, and documentation of statistical programs for use in creating analysis datasets, tables, listings, and figures.
Facilitate advanced technical expertise, in conjunction with internal and external team members, to design, implement, validate, and maintain project reporting applications that are supported by the department.
Assist in ensuring the optimum performance of group function.
May recommend and implement techniques to improve productivity, increase efficiencies, cut costs, take advantage of opportunities, and maintain state-of-the-art practices.
Work independently to carry out assignments with little direct supervision.
Identify project priorities and project timeline goals and communicate priority related issues and timelines to programming teams.
Ensure the efficiency, quality, and integrity of data reporting, and project activities executed.
Successfully represent the department and the company in sponsor meetings/presentations and maintain a positive working relationship with sponsors, collaborating associates, and vendor personnel.
Maintain awareness of project budgets and tasks, and effectively communicate the status of such tasks to line management and the project manager, as appropriate.
Perform other duties as required by the Department.
REQUIREMENTS:
I have an undergraduate degree or higher in Biostatistics, mathematics, Computer Science, or equivalent.
3 years of Statistical Programming/Statistics experience or an equivalent combination of education and experience to successfully perform the key responsibilities of the job.
3 years of one or more statistical software packages (SAS® preferred, and/or R and/or Python) used to conduct statistical analyses.
3 years working knowledge CDISC standards.
Previous experience in pharmaceutical research or CRO setting required.
Energized self-starter.
Excellent organizational skills.
Excellent communication skills, verbal and written.
Exceptional attention to detail.
Flexible, team player.
Proven ability to organize and effectively prioritize workload and deliverables.
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