Senior Manager, Statistical Programming

This is a fully remote position, open to applicants in United States.

📋 Description

• Develop all necessary tables, listings, and graphs for assigned clinical study reports (CSRs).

• Serve as the lead programmer for designated projects.

• Program tailored data displays in alignment with the approved statistical analysis plan (SAP) and shell displays for clinical research studies.

• Write code utilizing Base SAS programs, SAS procedures, or established macros.

• Analyze protocols, SAPs, and existing shells/templates to comprehend data structure and content.

• Conduct data checks to ensure the integrity and accuracy of data displays.

• Prepare documentation for programs, datasets, variables, derived variables, and projects.

• Generate SAS datasets of clinical data from clinical databases.

• Create status and efficacy datasets.

• Develop project-specific macros and formats.

• Import client data from various platforms and software packages.

• Prepare data for clients and facilitate external transfers/data imports.

• Communicate with clients to establish and manage project timelines and deliverables.

• Delegate projects to the team and address problems or technical challenges.

• Train junior team members on industry regulations, standards, and internal tools.

• Collaborate with IT to establish and maintain a secure environment with proper access control on SAS servers.

• Partner with Quality Assurance on drafting/revising Standard Operating Procedures and testing and validating CONFORM modules.

⛳️ Requirements

• Proficient communication skills in English, both written and verbal.

• Ability to quickly learn and maintain attention to detail.

• Capability to manage multiple tasks/projects, effectively prioritize and execute assignments, ensuring quality and timely deliveries.

• Ability to work collaboratively and productively within diverse organizational structures and in interactions with dynamic clients.

• Capacity to work independently, take ownership, and strive for quality and efficiency.

• Positive attitude in a continuously evolving environment.

• Strong/Advanced SAS skills and comprehension of standardization in data, programming, and statistical reporting of trial results and its implications for drug development.

• Master’s degree or higher in Biostatistics, Computer Science, Mathematics, or a combination of education and relevant industry experience.

• Proficient in SAS programming language with a solid understanding of clinical trials and drug development.

• Minimum of 2 years of clinical SAS programming experience for the managerial role.

• Some travel (5%) may be necessary, including potential weekend travel.

• Involvement in cross-functional interactions.

🏝️ Benefits

• A variety of comprehensive Medical, Vision, and Dental Insurance plans.

• Paid vacation time and sick leave.

• Annual corporate holidays.

• Participation in the 401K Plan.

• Extensive perks and discount programs for AAA, wholesale, insurance, Rx, fitness, pets, entertainment, and more.

• Access to Health Advocate and Employee Assistance Programs.