CSAR Manager - SAS Edit Check Programmer

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

Skills Required

Data Management, Gcp, Project Management, Sas Programming, Clinical Trials