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Senior Data Analyst
3 weeks ago
Advanced clinical development and statistical programming is crucial for the success of drug development.
Job OverviewThe Senior Statistical Programmer will have experience in all required areas of a Statistical Programmer II. They are responsible for providing expert programming support for clinical trials, ensuring that data analysis meets the highest standards of quality and accuracy.
Responsibilities:- Deliver high-quality programming solutions that meet or exceed client expectations.
- Develop and implement CDISC and other regulatory standards, maintaining a strong understanding of industry data standards.
- Follow internal SAS programming conventions, adhering to company procedures and guidelines.
- Serve as programming lead on assigned studies, coordinating activities with cross-functional teams.
- Coordinate and ensure the accuracy and completeness of activities for assigned support programmers, maintaining project timelines and ensuring timely completion.
- Create and maintain project schedules, identifying and addressing potential roadblocks.
- Support the development of tools and macros to improve quality and efficiency of processes, streamlining data analysis and reporting.
- Prepare programming specifications for SDTM, ADaM and other derived datasets, applying knowledge of SAS programming to develop and validate statistical outputs according to the statistical analysis plan and other specifications.
- Perform ad hoc analyses of current and legacy databases, reviewing and providing input on case report form design.
- Serve as a mentor to other programmers, guiding them on procedures and best practices.
- Maintain awareness of scope of work to actual work, alerting management of potential change orders or resourcing needs.
- Work effectively with other programmers, statisticians, data managers, database programmers and other cross-functional team members to ensure accurate and high-quality statistical outputs.
- Strong understanding of departmental and company procedures; ability to guide others on procedures.
- May assist in the preparation and review of monthly financial reports, promoting transparency and accountability.
- May promote visibility outside of the functional area, effectively interacting cross-functionally and in industry.
- May participate in candidate interviews, contributing to the hiring process.
- Perform other duties as requested by management, demonstrating flexibility and adaptability.
Qualifications:
- The ideal candidate should have a degree in Statistics, Computer Science, or a closely related field, with relevant work experience substituted for degree where applicable.
- Minimum of 4 years direct SAS programming experience in pharmaceutical development or CRO environment, with expertise in medical terminology and conduct and analysis of clinical trials.
- Good knowledge of relevant industry data standards (e.g. CDISC SDTM, ADaM, etc.).
- Excellent oral and written communication skills, organizational skills, and attention to detail required.
At Advanced Clinical, we value diversity and inclusion in every part of our organization, crucial to fulfilling our mission and demonstrating our values.
We seek talented individuals from diverse backgrounds and cultures to work with us, creating an inclusive workplace that appreciates valuable experience.
