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Amgen Inc

CSAR Manager - SAS Edit Check Programmer

9-12 Years
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Job Description

  • Support of clinical trial platform technologies
  • Support decision-making by acting as a data scientist bringing awareness to patterns and analytical insight
  • Coordinating and providing programming support to Clinical Study Teams
  • Works collaboratively with Clinical Data Management to meet study deliverables and timelines
  • Acting as a technical point of contact for systems deliverables on defined programs
  • Experience in creating/programming complex SAS edit checks according to specifications, testing them for functionality and identify potential issues before implementation.
  • Providing technical and business process input / expertise on new and emerging technologies
  • Develop, review and implement policies, SOPs and associated documents
  • Assist in preparing for and responding to audit findings (internal or external).

Basic Qualifications

  • Bachelors degree or equivalent in life science, computer science, business administration or related discipline with 9-13 years of experience
  • Proven experience in managing teams
  • Specialist knowledge / experience in life sciences or a medically related field
  • General biopharmaceutical clinical research experience (clinical research experience obtained working on clinical trials at a biotech, pharmaceutical or CRO company).

Preferred Qualifications

  • Advanced degree or equivalent in life science, computer science, math, statistics, business administration or related discipline with 9-13 years of experience
  • Broad knowledge / work experience in data management / programming in the Pharmaceutical or Biotech arena
  • Proven experience in managing teams
  • General project management and planning experience
  • Experience in oversight of outside vendors (CRO, central labs, imaging vendors, IRT vendors, etc.)

Knowledge

  • Good Clinical Practice
  • Strong understanding and experience in the use of performance management techniques, measures, problem-solving and analytical thinking
  • Drug development and clinical trials processes
  • Data management processes
  • Programming of clinical trial databases and applications
  • Proficient in SAS edit check programming
  • Systems development lifecycle
  • Programming Languages
  • Project planning and management
  • Collaborating with global cross-functional teams (team/matrix environment)
  • Quality management and Risk Analysis
  • Regulatory filings and inspections
  • Process improvement methodologies

More Info

Job Type:
Employment Type:
Open to candidates from:
Indian

About Company

Job ID: 111855725

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