Okay, I've searched for Director roles in Statistical Programming located in San Diego, CA within the biotechnology industry, requiring at least 8 years of experience and advanced SAS programming skills. I found 12 positions that match your criteria.

Sure. Here's the analysis:

Job Analysis:

The Associate Director/Director of Statistical Programming at Kura Oncology plays a pivotal role in advancing clinical development efforts within a biopharmaceutical landscape that demands precision and efficiency. The key purpose of this role is to provide technical leadership and strategic programming support, ensuring that statistical programming deliverables meet rigorous industry standards and regulatory requirements throughout a project’s life cycle—from study start-up through to submissions and post-marketing activities. Essential responsibilities include collaborating closely with project biostatisticians and CRO vendors, which underscores the importance of cross-functional coordination and building strong relationships. This candidate will face challenges like balancing timely delivery while maintaining quality, especially given the critical nature of clinical trials in the oncology sector. Success in this role is measured not just by technical outputs but also by fostering a culture of collaboration, maintaining high standards of quality assurance, and navigating the complex regulatory environment. The ideal candidate will leverage advanced programming skills, particularly in SAS, to create impactful solutions that contribute directly to improving patient outcomes in cancer treatment. Achieving objectives will require a keen understanding of both the technical aspects of programming and the broader strategic context of drug development.

Company Analysis:

Kura Oncology is positioned as an innovative player in the biopharmaceutical industry, dedicated to the development of precision medicine to treat cancer. As a clinical-stage organization, Kura is focused on translating cutting-edge biology into life-saving therapies, a mission that underscores the importance of agility, strategic thinking, and scientific rigor. The company operates in a highly competitive market, working with a pipeline that includes promising investigational drug candidates like ziftomenib and tipifarnib. This focus on targeted therapies reflects the industry's shift towards personalized medicine, which may add complexity to the role by necessitating continual learning and adaptation to emerging scientific data. Kura's culture appears to prioritize collaboration, integrity, and relentless execution, making it essential for the candidate to align with these values to thrive. The statistical programming role directly supports Kura's mission, positioning it as a key player in driving clinical success and compliance with regulatory demands. Given that the role functions within multidisciplinary study teams, high visibility with leadership and opportunities for significant influence are likely, providing a suitable environment for someone looking to make a meaningful impact while advancing their own professional growth within a mission-driven organization.

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

• Tell me about a time when you had to manage conflicting priorities in a clinical trial. How did you approach it?
• Can you describe a situation where you led a project from start to finish? What steps did you take to ensure success?
• Discuss a time when you identified and resolved a problem within a programming deliverable. What did you learn from that experience?
• Describe your experience with CDISC submission packages. How have you ensured adherence to their standards in past projects?
• How would you approach developing statistical programming standards for a new oncology drug trial?
• What methods do you use to validate programming deliverables and ensure compliance with regulatory requirements?
• Imagine you're given a tight deadline for data analysis needed for a clinical study report. How would you prioritize your tasks?
• Suppose you discover that a CRO vendor is behind schedule. How would you handle the situation to minimize impact on the project?
• Why are you interested in working at Kura Oncology specifically, and how does our mission resonate with your career aspirations?
• How do your values align with Kura's emphasis on collaboration and integrity in drug development?
• What are the key challenges you anticipate in this role, and how do you plan to address them?
• What do you think is the most critical factor for success when working in a multidisciplinary team in clinical trials?
• Can you share an example of how you leveraged AI or automation to enhance programming workflows in your previous roles?
• What questions do you have about the statistical programming team's structure and its collaboration with other functions at Kura?
• How do you keep yourself informed about the latest regulations and standards in clinical trial programming?