
Highly Skilled Senior Data Analyst
24 hours ago
Job Overview:
We are seeking a highly skilled and experienced Senior Statistical Programmer to join our team. This individual will play a key role in providing programming support for clinical trials, ensuring the accuracy and completeness of statistical outputs.
Responsibilities:
- Exceed expectations and responsibilities of a Statistical Programmer II
- Understand and implement industry data standards such as CDISC SDTM, ADaM, etc.
- Follow internal SAS programming conventions
- Serve as programming lead on assigned studies
- Coordinate and ensure the accuracy and completeness of activities for assigned support programmers.
- Create and maintain project timelines
- Support the development of tools and macros to improve quality and efficiency of processes
- Prepare programming specifications for SDTM, ADaM and other derived datasets
- Apply knowledge of SAS programming to program/develop and/or validate statistical outputs according to the statistical analysis plan and other specifications; including but not limited to:
- Analysis datasets (SDTM, ADaM, other derived datasets)
- Tables, listings and figures
- xml/Reviewer's Guide
- Integrated summaries
- Perform ad hoc analyses of current and legacy databases
- Review and provide input on case report form design
- Serve as a mentor to other programmers
- 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
- Standard Operating Procedures (SOPs)
- Strong understanding of departmental procedures; ability to guide others on procedures
- May participate in the development and revision of department SOPs
- Business Development
- May support the business development process; RFI completion, proposal development, bid defense participation, attendance at industry/scientific meetings, etc.
Additional Responsibilities:
- May assist in the preparation and review of monthly financial reporting
- May promote visibility outside of the functional area and effectively interact cross-functionally and in industry
- May participate in candidate interviews
- Perform other duties as requested by management
Qualifications:
- The ideal candidate should have a degree in Statistics, Computer Science, or a closely related field; work experience may be substituted for degree
- Minimum of 4 years direct SAS programming experience in pharmaceutical development or CRO environment
- Good knowledge of medical terminology and conduct and analysis of clinical trials
- Knowledge of relevant industry data standards (e.g. CDISC SDTM, ADaM, etc.)
- Excellent oral and written communication skills, organizational skills, and attention to detail are required
Our Commitment to Diversity and Inclusion:
At Advanced Clinical, our commitment to diversity and inclusion in every part of our organization is crucial to fulfilling our mission and demonstrating our REAL values. A diverse staff allows us to effectively draw on different perspectives and enhance our efficiency and effectiveness. We seek talented, creative individuals from a variety of backgrounds and cultures to work with us. It is our priority that our workplace be inclusive, welcoming of diverse ideas and appreciative of valuable experience.
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