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Senior Sas Programmer

2+ years
Not Disclosed
10 Dec. 27, 2024
Job Description
Job Type: Full Time Education: B.Sc./M.Sc./B.Pharm/M.Pharm/Life science 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: Senior SAS Programmer

Location: Multiple Locations
Company: [Company Name]


Job Overview:

We are seeking a highly skilled Senior SAS Programmer to join our growing team. The Senior SAS Programmer will be responsible for providing SAS programming support for TFL generation, performing statistical and programming tasks, and validating datasets for clinical trials. This role offers an excellent opportunity to work on both standard and ad-hoc SAS macros, review clinical research forms (CRF/aCRF), and contribute to the validation of critical datasets such as ADaM and SDTM.


Key Responsibilities:

  • TFL Generation: Provide programming support for generating Tables, Listings, and Figures (TFL) based on clinical trial data.
  • CRF Design and Review: Contribute statistical/programming inputs for CRF design, ensuring they align with the study objectives.
  • SAS Macros Development: Develop and validate standard and ad-hoc SAS macros to streamline programming processes.
  • CRF and aCRF Review: Perform thorough reviews of CRF and aCRF to ensure completeness and consistency.
  • Statistical Analysis Plans: Review and provide inputs on statistical analysis plans (SAPs) to ensure alignment with study objectives and data analysis strategies.
  • Efficacy Variables Programming: Prepare programming specifications for efficacy variables to ensure accurate data reporting.
  • Safety Tables Validation: Validate the Safety Tables using SAS to ensure data accuracy and regulatory compliance.
  • ADaM and Derived Datasets: Prepare and validate ADaM and derived datasets, ensuring data is correctly processed and ready for analysis.
  • SDTM Datasets Validation: Validate SDTM datasets and their specifications to ensure proper transformation of raw clinical data into standard formats.
  • Training and Development: Adhere to required training and actively engage in professional development to stay up-to-date with the latest industry practices.

Qualifications:

  • Educational Background:
    • Bachelor's degree in a relevant field (e.g., Computer Science, Statistics, Life Sciences).
  • Experience:
    • Minimum of 5 years of experience as a SAS programmer in a clinical research environment.
    • Strong experience in TFL generation, ADaM, SDTM, and SAS macro development.
    • In-depth knowledge of clinical trial datasets and statistical analysis plans.
    • Experience working with efficacy variables, safety tables, and CRF/aCRF review.
  • Skills:
    • Proficiency in SAS programming, including advanced skills in macros, statistical analysis, and data validation.
    • Experience with clinical trial data management, specifically for ADaM, SDTM, and TFL generation.
    • Strong understanding of clinical research processes, regulatory requirements, and good clinical practice (GCP).
    • Attention to detail and ability to work independently and in a collaborative team environment.

Desired Attributes:

  • Strong analytical and problem-solving skills.
  • Ability to prioritize tasks in a fast-paced environment.
  • Effective communicator with the ability to interact with multidisciplinary teams.
  • Commitment to quality and continuous learning in the field of clinical programming.

Why Join Us?

  • Exciting Career Development: Opportunities for career advancement in clinical programming and SAS development.
  • Impactful Work: Be part of a team contributing to groundbreaking work in clinical research, helping to bring new treatments to market.
  • Collaborative Environment: Work alongside experienced professionals in a supportive and innovative environment.
  • Competitive Compensation & Benefits: Receive an attractive salary package, along with benefits such as health insurance, paid leave, and retirement plans.

How to Apply:

If you are a skilled Senior SAS Programmer looking to take the next step in your career, we encourage you to apply today. Please submit your resume and application through [company's career portal] or email us directly at [contact email].


Equal Opportunity Employer:

We are committed to providing equal opportunities to all candidates. We value diversity and inclusion and encourage individuals from all backgrounds to apply.


Join our team and contribute to advancing clinical research with your SAS programming expertise!