Okay, I've searched for Statistical Analyst roles in Miami, specifically for contract positions that require over 6 years of experience, focusing on SAS programming and drug development with an understanding of CDISC standards. I have found 32 positions for you.

Sure. Here's the analysis:

Job Analysis:

The primary focus of the Statistical Analyst role at Katalyst CRO is to lead statistical programming activities for clinical trials, particularly in creating outputs such as Adam datasets, tables, listings, and figures that conform to CDISC standards. This responsibility involves not just technical proficiency in SAS programming but also an understanding of the drug development process, regulatory requirements, and the ability to collaborate with team members to ensure quality and compliance. Success in this role means producing high-quality statistical outputs with precision and clarity while mentoring junior team members and contributing to standard operating procedures. Candidates will likely face challenges related to managing complex datasets and meeting regulatory deadlines, necessitating strong organizational and communication skills to navigate these effectively.

Company Analysis:

Katalyst CRO is positioned within the healthcare and life sciences industry as a comprehensive contract research organization. The company emphasizes a client-centric approach and aims to innovate within research and regulatory compliance, showcasing its commitment to advancing healthcare solutions. Cultural indicators suggest a dynamic and quality-driven environment, where employees are expected to be proactive in their responsibilities and contribute to the organization's goals of improving patient health outcomes. In the organizational hierarchy, the Statistical Analyst plays a critical role in data management and analysis, with significant visibility due to the regulatory nature of the work. This position aligns with Katalyst's larger strategic goals of efficiently bringing therapies to market, thus making it essential for candidates to not only possess the required technical skills but also to demonstrate an appreciation for the critical impact of their work on patient safety and regulatory success.

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

• Tell me about a time when you had to lead a statistical programming project. What challenges did you face and how did you overcome them?
• Can you describe a situation where you had to mentor a junior programmer? How did you approach their development and what was the outcome?
• Describe a project where your estimate of programming efforts proved to be inaccurate. What did you learn from that experience?
• How would you ensure that your SAS programs are compliant with CDISC standards in the data you are working with?
• What steps would you take to validate Adam datasets and ensure they meet regulatory standards?
• Can you walk us through your process for creating documentation for regulatory filings?
• Imagine you have conflicting priorities between two projects you are leading. How would you manage your time and keep both stakeholders informed?
• Why do you want to work at Katalyst CRO specifically, and how do you think your skills align with our mission?
• How would you approach creating standard SAS Macros for use across multiple projects?
• What do you think is the most critical aspect of statistical programming in the context of drug development?
• Do you have any questions for us about Katalyst CRO's approach to innovation in research?
• What further support or resources do you think you would need to thrive in this role?