Okay, I've searched for Statistical Programmer roles in New York County, NY, specifically within the pharmaceutical industry, requiring 5+ years of experience, with a focus on SAS programming. I have found 27 positions for you.

Sure. Here's the analysis:

Job Analysis:

The Statistical Programmer role at Katalyst CRO is fundamentally about providing critical programming support for clinical trials in the pharmaceutical industry. The primary responsibilities include developing and validating SAS programs to analyze clinical trial data, ensuring accuracy and adherence to regulatory standards. Collaboration with multiple stakeholders like Biostatisticians and Data Managers is essential, illustrating the need for effective cross-functional coordination. Candidates can expect to face challenges related to data inconsistency and regulatory compliance, necessitating a strong problem-solving skill set. Success in this role would manifest as the timely delivery of accurate datasets that meet quality standards, thereby supporting informed decision-making in clinical trials.

Company Analysis:

Katalyst CRO operates in the dynamic and highly regulated intersection of healthcare and life sciences, providing extensive research and regulatory solutions to enhance drug development processes. As a forward-thinking organization, it embraces a culture of innovation and collaboration, which is vital for roles like the Statistical Programmer that require teamwork and adaptability in a fast-paced environment. Given the company’s focus on advancing healthcare through quality excellence and regulatory success, the role aligns with broader organizational goals of optimizing the drug development lifecycle. Katalyst seems to prioritize expertise and flexibility, which allows employees to contribute meaningfully to critical healthcare advancements.

Absolutely. Here are some mock interview questions that could come up:

• Describe a time when you had to ensure the accuracy of a dataset. What steps did you take?
• Can you give an example of a complex problem you faced during a clinical trial and how you resolved it?
• Tell me about a situation where you collaborated with a diverse team to achieve a common goal.
• How do you prioritize tasks when working on multiple projects with tight deadlines?
• How would you approach developing a SAS program for a clinical trial dataset?
• What strategies do you use to maintain programming standards and documentation?
• Can you walk us through the process you follow for quality control checks in your data analysis?
• Imagine you discover a significant discrepancy in the trial data close to a submission deadline. What would you do?
• Why are you interested in working at Katalyst CRO, specifically?
• How do you see your role as a Statistical Programmer contributing to Katalyst's mission to advance healthcare?
• What specific experiences do you have with CDISC data standards in your previous roles?
• What questions do you have about the team's culture or the projects you would be working on?