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Senior Statistical Programmer (Argentina)

7+ years
Not Disclosed
10 Jan. 30, 2025
Job Description
Job Type: Full Time Education: BA/BS/BCS 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

๐ŸŒŸ Now Hiring: Senior Statistical Programmer - Argentina ๐Ÿ‡ฆ๐Ÿ‡ท

๐Ÿ’ผ Position: Senior Statistical Programmer
๐Ÿข Industry: CRO - Biometrics
๐Ÿ“ Location: Argentina
โณ Job Type: Full-time

๐Ÿ”Ž Job Overview

The Senior Statistical Programmer will be responsible for leading clinical trials, developing and validating annotated Case Report Forms (aCRFs), SDTM datasets, ADaM datasets, and TLFs, ensuring compliance with regulatory requirements and industry standards. You will also review documents such as SAPs, TLF Shells, and Data Management (DM) documents, while supporting data cleaning activities and collaborating with cross-functional teams.

๐Ÿ”‘ Key Responsibilities

1. Programming & Validation

  • Lead statistical programming for single and multiple clinical trials
  • Develop/maintain/validate aCRFs, SDTM, ADaM datasets, and TLFs
  • Ensure adherence to CDISC standards and regulatory guidelines

2. Data Management & Quality

  • Support DM with data cleaning and resolving statistical data issues
  • Use global SAS macros for efficient programming of datasets and TFLs
  • Validate SDTMs, ADaMs, and define.XMLs using Pinnacle 21

3. Collaboration & Mentorship

  • Collaborate with Biostatistical study teams to deliver high-quality outcomes
  • Mentor junior Statistical Programmers and provide guidance

4. Continuous Improvement

  • Participate in internal initiatives to improve programming efficiency and quality
  • Keep up-to-date with the latest industry standards and regulations

๐Ÿ“Œ Requirements

๐ŸŽ“ Education:

  • Bachelor’s degree in Statistics, Computing Sciences, or related field; Master’s degree a plus

๐Ÿ›  Experience:

  • At least 7 years of clinical research experience, with 5 years in Statistical Programming and 2 years as Lead Statistical Programmer

๐Ÿ’ป Skills:

  • Strong knowledge of clinical trial data, SAP, TLF Shells, and CDISC standards
  • Proficiency in SAS programming; SAS certification an asset
  • Knowledge of XML programming and ICH guidelines
  • Excellent organizational, project planning, and time management skills
  • Strong communication skills in English

๐ŸŽฏ Perks & Benefits

โœจ Flexible home-based work schedule
โœจ Ongoing learning and development opportunities
โœจ Collaborative work environment

๐Ÿ“Œ Company: Innovaderm (Specialized in Dermatology CRO Research)

๐Ÿ“ฉ Apply Now!