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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

🌟 Now Hiring: Senior Statistical Programmer - Argentina 🇦🇷

💼 Position: Senior Statistical Programmer
🏢 Industry: CRO - Biometrics
📍 Location: Argentina
Job Type: Full-time

🔎 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.

🔑 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

📌 Requirements

🎓 Education:

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

🛠 Experience:

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

💻 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

🎯 Perks & Benefits

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

📌 Company: Innovaderm (Specialized in Dermatology CRO Research)

📩 Apply Now!