Senior Statistical Programmer/Analyst Consultant

📋 Description

• Accountable for assisting with the Programming deliveries of a clinical study or project.

• Executes statistical programming components of the protocol and the clinical development program.

• Guarantees high quality in personal deliverables and in the work produced by other programmers.

• Programs autonomously with a focus on high efficiency and quality.

• Drafts and/or applies specifications while ensuring the completeness of pertinent documentation.

• Aids in the formulation of best practices aimed at enhancing quality, efficiency, and effectiveness within the function.

• Ensures adherence to standards and the utilization of automation.

• Organizes and supports team activities and assignments.

• Communicates and escalates risks associated with the assigned studies and/or projects.

• Collaborates proactively with study team members, including but not limited to the Statistician, Lead Programmer, Data Manager, and Study Leader.

⛳️ Requirements

• Bachelor's degree in computer science (CS), statistics, or related scientific disciplines, accompanied by 5 years of clinical programming (CDISC) experience.

• Oncology therapeutic area experience is required.

• Familiarity with ICH and Good Clinical Practices, clinical research, clinical trial processes, and associated regulatory requirements and terminology.

• Solid comprehension of the clinical drug development process.

• Excellent communication and coordination skills.

• Up-to-date knowledge of technical and regulatory requirements pertinent to the role.

• Ability to proactively manage multiple activities within a project.

• Proficient in influencing relevant stakeholders regarding programming-related matters.

🏝️ Benefits

• Flexible work arrangements.

• Opportunities for professional development.