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Sr. Biostatistician

3-4 years
Not Disclosed
10 Dec. 5, 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 Description: Senior Statistical Programmer

Job Overview:
We are seeking an experienced Senior Statistical Programmer to provide technical expertise and leadership in developing process methodologies to meet the needs of both internal and external clients. This role will involve planning and coordinating integrated programming solutions for statistical programming needs, providing internal consulting, and handling complex project requirements.

Essential Functions:

  • Lead and coordinate programming, testing, and documentation for complex studies, including statistical tables, figures, listing summaries, and analysis databases (derived datasets).
  • Program and integrate databases from multiple studies or sources.
  • Develop and coordinate programming documentation, including plans and specifications for complex studies.
  • Provide advanced technical expertise and bring solutions for complex studies in collaboration with internal and external clients.
  • Plan, develop, implement, and validate new process technologies, macros, and applications.
  • Serve as the statistical team lead for single complex studies or a group of studies.
  • Manage project scope, budget, resource forecasts, and provide revenue forecasts.
  • Provide training and guidance to junior staff members.

Qualifications:

  • Master’s degree in Computer Science or related field with 3 years of relevant experience, or
  • Bachelor’s degree in Computer Science or related field with 4 years of relevant experience.
  • Equivalent combination of education, training, and experience may be considered in lieu of a degree.
  • Strong knowledge of statistics, programming, and the clinical drug development process.
  • Advanced proficiency in SAS (Base SAS, SAS Graph, SAS Macro Language).
  • Excellent organizational, interpersonal, leadership, and communication skills.
  • Ability to manage multiple tasks and projects with high accuracy and attention to detail.
  • Strong relationship-building skills with coworkers, managers, and clients.

About IQVIA:
IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence. We accelerate the development and commercialization of medical treatments to improve patient outcomes and population health worldwide.

Learn More and Apply: https://jobs.iqvia.com