Katalyst HealthCares & Life Sciences

Clinical SAS Programmer

Katalyst HealthCares & Life Sciences South Plainfield, NJ
Katalyst HealthCares & Life Sciences

Clinical SAS Programmer

Katalyst HealthCares & Life Sciences South Plainfield, NJ
2 months ago 58 applicants

See who Katalyst HealthCares & Life Sciences has hired for this role

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.

  • Seniority level

    Mid-Senior level

  • Employment type

    Contract

  • Job function

    Information Technology

  • Industries

    Pharmaceutical Manufacturing

Referrals increase your chances of interviewing at Katalyst HealthCares & Life Sciences by 2x

See who you know

Get notified about new SAS Developer jobs in South Plainfield, NJ.

Sign in to create job alert

Similar jobs

People also viewed

Similar Searches

Explore collaborative articles

We’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI.

Explore More