Qualifications

• Bachelor or Master degree in a related field (Computer Science, Mathematics, Engineering, Medical).
• 5+ years of experience with statistical programming (SAS, R) in the pharmaceutical industry (or 3+ years with a Master's).
• Strong proficiency in SAS, including SAS Macro language.
• Experience with R programming in the context of clinical trials.
• Familiarity with the drug development process and industry standards.
• Ability to manage data integrations (ISS and ISE).
• Excellent communication skills, capable of conveying technical details to non-technical team members.

Responsibilities

• Lead programming for clinical trials by deriving datasets and validating tables, figures, and listings.
• Conduct ad hoc exploratory analyses to support research publications and programming.
• Oversee programming work and deliverables from Contract Research Organizations (CROs).
• Contribute to the design and review of critical documentation (e.g., Statistical Analysis Plan, SDTM/ADaM specifications).
• Program and validate CDISC compliant electronic submissions and support documentation creation.
• Manage programming deliverables to meet timelines and ensure high-quality output.
• Participate in developing departmental working instructions and create enhanced programming functions.

Benefits

• Remote work flexibility to accommodate personal circumstances.
• Participation in the development of company standards and guidelines to enhance your skills.
• Opportunity to lead programming efforts and provide mentorship to junior programmers.
• Involvement in cross-functional collaborations, enhancing your exposure to different departments.
• Support with professional development in the pharmaceutical programming sector.