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Statistical Programmer at Katalyst HealthCares & Life Sciences

unlimited holidays - extra holidays - extra parental leave - long remote period allowed
Remote: 
Full Remote
Experience: 
Senior (5-10 years)
Work from: 
United States

Offer summary

Qualifications:

5+ years of programming experience, Bachelor's/Master's Degree in Computer Science, Engineering, Mathematics, or Statistics, Experience with SAS programming and certification, Familiarity with relational database structure and reporting systems.

Key responsabilities:

  • Implement and execute programming standards
  • Support clinical studies requests for statistical analyses
  • Provide documentation and maintenance of code
  • Follow company SOP and guidelines
  • Perform other duties as needed
Katalyst HealthCares & Life Sciences logo
Katalyst HealthCares & Life Sciences Pharmaceuticals SME https://www.katalysthls.com/
51 - 200 Employees
About Katalyst HealthCares & Life Sciences
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
See more Katalyst HealthCares & Life Sciences offers

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

Required profile

Experience

Level of experience: Senior (5-10 years)
Industry :
Pharmaceuticals
Spoken language(s):
Check out the description to know which languages are mandatory.

Hard Skills

Relational Database DesignSAS Macros

Other Skills

  • Social Skills
  • Verbal Communication Skills
Are you interested?

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