Clinical SAS Programming

Clinical SAS programming

Location: Remote

Immediate/15 D notice

Experience: 10+ years

Looking for a candidate who is into Clinical programming and report generation (excluding ADaM, SDTM, and TLF) who will be supporting data management team. (Candidates)clinical programmers play a crucial role in creating accurate reports. However, a significant challenge is that 1 in 3 candidates may be fake.

• Experience of Creating missing pages, patient profile reports, reconciliation reports
• Programming: BASE SAS, macros, SQL.
• Regulatory Knowledge: FDA, EMA, ICH guidelines.
• Soft Skills: Attention to detail, communication, problem-solving.
• BASE SAS Certified is Plus
• candidates should have created SAS reports for DM function.( E.g., missing pages report, reconciliation report, patient profiles etc).

Key requirements:

1) SAS Programmers with a minimum of 10 years of experience in clinical SAS programming. Python is good to have skillset.

2) Min 5 years of SAS experience with good understanding of DM and clinical stake holder requirements.

Additional details:

• Responsibilities include (but not limited to) design, development, implementation, and validation of programs created in SAS dashboard applications, to process, analyze and report clinical trial data for review by clinical study teams.
• Works within established frameworks and ensures high quality is built into own deliverables.
• Works independently for well-defined scope of work
• Under guidance, creates catalogue of reports to aid data cleaning activities with moderate scope and medium complexity, but not limited to:
• Automate manual checks.
• Automate reconciliation and program edit checks for TPV data to ensure quality.
• Create tools and repository to minimize data errors at source for collection of lab reference ranges.
• Program reports to identify missing pages and also detect errors at Subject level.
• Create reports to measure metrics that can help assess data cleaning status.
• Create visualizations and dashboards to identify discrepancies in EDC and TPV data.
• Maintain created catalogue of reports and perform updates based on ongoing changes to requirements.
• Provide support as required to ensure availability and performance of developed reports and dashboards for

both external and internal users

• Responsible for completion of documentation associated with programming tasks (e.g. peer review, report

specifications etc.) in compliance with applicable SOPs

• Proactively keeps the lead programmers updated on progress of deliveries.

Contribute to implementation of cross-functional projects that are part of clinical programming roadmap.