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Programmer Analyst - Sas

3+ years
Not Disclosed
10 Dec. 9, 2024
Job Description
Job Type: Full Time Education: MS/MA Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Job Title: Programmer Analyst - SAS

Location: Flexible
Work Schedule: Standard (Mon-Fri)
Environmental Conditions: Office


Position Summary

Join Thermo Fisher Scientific Inc. as a Programmer Analyst - SAS, where your expertise in SAS programming and data management will be instrumental in advancing clinical research projects. This role focuses on preparing and analyzing clinical trial datasets, ensuring data quality, and collaborating with multi-disciplinary teams to develop computational strategies tailored to bioinformatics research.


Key Responsibilities

Programming and Data Management

  • Develop, execute, and validate SAS programs to transfer, merge, and summarize data from multiple sources.

  • Prepare and analyze clinical trial datasets, including laboratory, vital signs, tumor response, imaging, and questionnaire data.

  • Generate reports and summaries using SAS and standard programming tools for clinical research applications.

Project Leadership and Consultation

  • Act as the programming lead for studies of simple to moderate complexity, overseeing project deliverables under supervision.

  • Collaborate with researchers and project teams to design technology-based solutions tailored to specific study requirements.

  • Provide input on project specifications, including SDTM and ADaM derivations.

Tool Development and Quality Assurance

  • Develop customized SAS code and validate outputs for clinical bioinformatics or technical use.

  • Ensure adherence to departmental SOPs and working practices while contributing to informal training and mentoring for team members.

  • Participate in developing quality control support for statistical programming and capture biostatistical metrics.

Professional Development

  • Enhance skills in programming, clinical trials, and pharmaceutical industry standards through collaboration, mentorship, and participation in department activities.

  • Contribute to departmental documents, policies, and presentations.


Qualifications

Education

  • Master’s degree in computer science, statistics, biostatistics, mathematics, or a related field.

  • Bachelor’s degree in a related field with at least 3 years of relevant experience will also be considered.

Experience

  • Proven ability to lead programming activities for project teams.

  • Experience developing specifications for SDTM and ADaM derivations.

Skills and Knowledge

  • Proficiency in SAS programming and familiarity with relational database structures.

  • Strong attention to detail, problem-solving skills, and ability to manage multiple assignments with tight timelines.

  • Excellent communication and collaboration skills, with a positive attitude and adaptability to changing priorities.

  • Understanding of clinical trials, pharmaceutical industry practices, and biostatistical metrics.


Why Join Us?

Thermo Fisher Scientific Inc. provides a dynamic and collaborative environment where innovation and dedication converge to make a significant impact on the healthcare industry. As a Programmer Analyst - SAS, you'll have the opportunity to work on meaningful projects, grow your skills, and contribute to improving global health outcomes.

If you’re a motivated professional with a passion for programming and clinical research, apply today to join our team!