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2+ years
Not Disclosed
10 Dec. 19, 2024
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences 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: Technical Officer - SAS Programmer
Location: Ahmedabad, India
Company: Lambda Therapeutic Research Ltd.
Date: Dec 15, 2024

Organizational Overview

Lambda Therapeutic Research Ltd. is a global leader in clinical research services, headquartered in Ahmedabad, India. With over 1500 employees across various international locations, Lambda provides a full spectrum of clinical trial solutions for the biopharmaceutical and generic industries. The company combines industry expertise, innovative technology, and a commitment to quality to support clients in developing safe, effective, and quick solutions for their products.

Job Details

As a SAS Programmer at Lambda Therapeutic Research Ltd., you will play a critical role in the clinical data management and biostatistics departments. You will work on clinical trial datasets, ensuring proper SAS programming in compliance with clinical study requirements and CDISC standards.

Key Responsibilities

  • SAS Programming: Perform CDISC-compliant SAS programming for both early-phase (BA/BE) and late-phase (CT) clinical trials.
  • Dataset Generation: Develop datasets (SDTM & ADaM) to support clinical trial data management.
  • Documentation: Generate essential CDISC documentation, including define.xml, CSDRG & ADRG, and aCRF.
  • QC and Review: Conduct programmatic quality checks for SAS deliverables using Pinnacle Validator software. Review eCRF annotations and collaborate with the CDM & Clinical teams for study data listings.
  • Team Management: Oversee team activities, ensure resource management, and provide training for quality improvement steps.
  • Project Management: Manage overall project timelines for CDISC SAS deliverables.

Key Deliverables

  • Successful generation and validation of datasets (SDTM & ADaM) for clinical trials.
  • Creation and submission of complete CDISC documentation (define.xml, CSDRG, etc.).
  • Timely delivery of SAS programming tasks while ensuring data quality.
  • Efficient management and oversight of team responsibilities.

Experience

  • Experience: At least 1 year of experience working as a SAS programmer in the clinical research or life sciences domain.
  • Skills: Expertise in CDISC SAS programming and dataset generation, including SDTM and ADaM.

Educational Qualifications

  • Certification: SAS® Base or Advanced Certification (mandatory).
  • Degree: Post-graduate degree in Science, Statistics, or Pharmacy.
  • Communication: Fluency in verbal and written English and Hindi.

Competencies

  • Strong accountability, communication, and work ethic.
  • Proactive initiative and leadership skills.
  • In-depth technical knowledge in SAS programming and clinical data management.
  • Strong presentation and interpersonal communication skills.
  • Ability to manage resources and organize work effectively.

Why Lambda?

Lambda offers a collaborative and innovative work environment, ideal for professionals looking to contribute to cutting-edge clinical research and data management processes. If you're passionate about making an impact in the clinical trials domain, Lambda provides the perfect platform for your career growth.