Senior Statistical Programmer

ROLES and RESPONSIBILITIES:

• Perform review of Protocol, Case Report Forms, annotated Case Report Forms, Statistical Analysis Plan, and mock shell
• Develop and/or validate SDTM domains and ADaM datasets as per the specifications for both Safety and efficacy

•Develop and/or validate Tables, Listings, and Figures using SAP and mock shells

•Create or review P21 reports, define packages [Define.xml] and Reviewers guide [RGs] for CDISC Data Standards

•Ability to work independently and as part of a team environment

•Provide the status of assigned tasks to the Study Lead Programmer

•Actively participating in the study meetings and support as backup lead

•Identify, communicate, and manage study-based risks and issues within the timeframe

•Maintain supporting documentation for studies in accordance with SOPs, and Work Instructions (WI) to ensure traceability and regulatory compliance

•Contribute to the development of Statistical Programming standards and processes to improve the quality, productivity, and efficiency

• Adhere to learning and developing knowledge on the latest in CDISC Therapeutic standards, GCP, and applicable ICH guidelines

•Provide guidance, mentoring, and training for junior team members as appropriate