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Clinical SAS Programmer

75% Flex
Remote: 
Full Remote
Experience: 
Senior (5-10 years)
Work from: 
Connecticut (USA), Illinois (USA)

Offer summary

Qualifications:

8 years of SAS programming experience in clinical trial data analysis, preferably in UNIX environment., Deep knowledge of CDISC Standards, ADaM programming, and Oncology TA experience..

Key responsabilities:

  • Support ISS, Client ADaM programming, and submissions.
  • Learn internal macros, processes, interpret Pinnacle 21 results.
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

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Your missions

Responsibilities and Requirements:
  • 8 years of experience in clinical trial data analysis using SAS. Preferably in UNIX environment Familiar with Unix command and environment.
  • Deep knowledge of CDISC Standards and solid ADaM programming experience. Oncology TA experience is preferred.
  • Ability to quickly learn internal macros, processes and interpret Pinnacle 21 results.
  • Experienced in supporting ISS, Client ADaM programming and submissions is a plus.
  • Team player with excellent communication skills and experience working with stat programmers, statisticians and data management personnel.
  • SAS programming, familiar with SAS language modules e.g. SAS MACRO, BASE, SGPLOT, SQL.
  • Working knowledge of macro programming; Be able to write macros and able to comprehend existing macros.
  • Derived Dataset derivation; knowledgeable about the definition or specification files.
  • High degree of technical competence and communication ability, both oral and written.
  • Pharmaceutical or related industry experience with clinical trials.

Required profile

Experience

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

Hard Skills

Clinical TrialsSASCDISC StandardsADAMUNIX

Soft Skills

  • Excellent Communication
Are you interested?

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