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Manager, CSAR - SAS Edit Check Programmer Job Opening In India, India – Now Hiring Confidential


Job description

Responsibilities include, but are not limited to, the following: 

  • 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)

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

What we expect of you 

We are all different, yet we all use our unique contributions to serve patients.

Preferred Qualifications 

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

Basic Qualifications 

  • Bachelor's degree or equivalent in life science, computer science, business administration or related field with6 to 8years of experience.
  • Master's degree and 4 to 6 years of experience.
  • 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)

Skills Required
Data Management, Vendor Management, System Development, Sas, drug development, Project Planning

Required Skill Profession

Computer Occupations


  • Job Details

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