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Senior / Principle Statistical Programmer

5+ years
Not Disclosed
10 Feb. 24, 2025
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: Senior / Principal Statistical Programmer
Location: Remote (India)
Job Type: Permanent

Job Description:

Clinovo is seeking a Senior / Principal Statistical Programmer to provide technical expertise and leadership within the Statistical Programming (SP) department. The role involves planning and coordinating programming solutions for complex clinical studies, creating statistical tables, figures, and datasets. The position also entails providing internal consulting services, developing specifications, and ensuring project deliverables meet internal and external client needs. As a leader, the Senior/Principal Statistical Programmer will mentor team members and communicate directly with internal and external clients.

Responsibilities:

  • Lead and coordinate programming, testing, and documentation of statistical programs for creating tables, figures, and listings.

  • Program analysis datasets and transfer files for internal and external clients.

  • Implement quality control checks for source data and report any issues.

  • Develop programming specifications for complex studies and collaborate with client and internal statisticians.

  • Manage project timelines, resource assignments, and ensure deliverables meet deadlines.

  • Use and promote best practices, SOPs, and established standards.

  • Train and mentor team members within the Statistical Programming department.

Preferred Skills and Experience:

  • Experience: Statistical programming in SAS within CRO, Pharmaceutical, Biotechnology, or Healthcare industries.

  • Technical Leadership: Ability to lead teams, engage with clients, and manage programming tasks.

  • Regulatory Knowledge: In-depth knowledge of clinical research regulatory requirements (GCP, ICH guidelines).

  • Programming Skills: Advanced proficiency in Base SAS, SAS/STAT, SAS Graph, SAS Macro Language.

  • Project Management: Ability to estimate programming scope, manage resources, and negotiate timelines.

  • Problem-Solving: Ability to solve complex problems and negotiate when necessary.

Requirements:

  • Education:

    • Master’s degree in Computer Science or related field with 3 years of relevant experience, OR

    • Bachelor’s degree or equivalent in Computer Science or related field with 5 years of relevant experience, OR

    • Equivalent combination of education, training, and experience.

Compensation:

Compensation will depend on relevant work experience, skills, and years of experience.