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Senior Statistical Programmer

Ergomed
Ergomed
8-10 years
Not Disclosed
10 April 24, 2025
Job Description
Job Type: Full Time Education: BCS/B..Tech 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 Statistical Programmer
Location: Remote
Employment Type: Full-time
Department: Biostatistics


About the Company:

Ergomed Group is a rapidly expanding full-service mid-sized CRO with a strong focus on Oncology and Rare Diseases. Founded in 1997, Ergomed has consistently grown through strategic investments and acquisitions. With a presence across Europe, North America, and Asia, we foster a collaborative and inclusive international work culture, emphasizing employee well-being, creativity, and professional development.


Job Responsibilities:

  • Lead statistical programming activities for clinical studies and programs, ensuring timely and high-quality deliverables

  • Develop SDTM and ADaM datasets and specifications

  • Generate CDISC submission packages, including Define.xml and Reviewers Guide

  • Program tables, listings, and figures (TLFs) using SAS based on study specifications

  • Conduct quality control (QC) procedures to ensure first-time quality of datasets and outputs

  • Act as a programming expert, providing guidance and consultative support to colleagues and stakeholders

  • Represent programming needs in cross-functional meetings and audits

  • Mentor and train junior statistical programmers and contribute to process improvement initiatives

  • Participate in departmental planning, including work projections and innovation in programming solutions


Required Qualifications:

  • Bachelor's degree in Computer Science, Mathematics/Statistics, or a related quantitative field

  • 8–10 years of experience in clinical research statistical programming

  • Proficient in SAS Base, Macro, and ODS

  • Advanced knowledge of CDISC standards and submission requirements

  • Hands-on experience with P21E and clinical data submission workflows

  • Strong organizational and multitasking skills

  • Excellent verbal and written communication abilities

  • Proficiency in Microsoft Office and one or more statistical programming languages (SAS, R)


What We Offer:

  • Internal training and career development programs

  • Emphasis on both personal and professional growth

  • Friendly and supportive global work environment

  • Opportunities to collaborate with international teams using English as the company language


Core Values:

  • Quality

  • Integrity & Trust

  • Drive & Passion

  • Agility & Responsiveness

  • Belonging

  • Collaborative Partnerships