Sr Programmer Analyst

Standard (Mon-Fri) Environmental Conditions Office Job Description Senior Programmer Analyst Join Us as a Senior Programmer Analyst – Make an Impact at the Forefront of Innovation The Senior Programmer Analyst performs advanced bioinformatics programming activities supporting the statistical and computational aspects of clinical research projects.

Works independently as a Lead Programmer on moderately complex studies. Serves as a study team member under the direction of a Lead Programmer on more complex studies.

Responsibilities

• Provides training, guidance, and mentoring to junior team members.
• Programming & Bioinformatics Activities Independently create, execute, maintain, and validate programs that: Transfer data across multiple data management systems or operating systems.
• Combine data from a variety of sources and structures.
• Generate and store summary data from multiple sources.
• Generate reports or combine multiple databases.
• Validate programs that generate listings, tables, and figures using SAS.
• Study Leadership & Project Management Act as the Lead Programmer on selected studies of moderate complexity.
• Collaborate directly with project team leaders and client representatives.
• Assess and develop project goals and timelines.
• Assume leadership responsibilities as a contributing member of multidisciplinary clinical trial project teams.
• Communicate proactively with cross-functional team members to ensure project success.
• Assignment & Quality Management Manage and document assignments to meet project timelines and quality expectations.
• Ensure compliance with relevant contractual obligations and project requirements.
• Perform quality control reviews of statistical programming deliverables.
• Training & Development Continuously enhance expertise in programming technologies, clinical trials, and the pharmaceutical industry.
• Train, mentor, and guide junior programmers.
• Support knowledge sharing within the team.
• & Strategic Support Support departmental initiatives and infrastructure by: Representing the company at industry conferences.
• Presenting at internal department meetings.
• Assisting in the development of training materials.
• Contributing to departmental documents, policies, SOPs, and working practice documents.
• Supporting proposal and bid activities as requested.

Requirements

• & Experience Requirements Required Qualifications Master's Degree in Computer Science, Statistics, Biostatistics, Mathematics, or a related field with a minimum of 6 years of relevant experience OR Bachelor's Degree in Computer Science, Statistics, Biostatistics, Mathematics, or a related field (or an equivalent relevant academic/vocational qualification) with a minimum of 6 years of relevant experience.
• Relevant experience should demonstrate the knowledge, skills, and abilities required to perform advanced statistical programming, bioinformatics programming, and clinical trial support responsibilities.
• Years of experience should be considered alongside technical expertise, leadership capability, and overall proficiency, rather than as the sole selection criterion.