Scientific/Medical Director, Medical Affairs – Hematology/Oncology

The Scientific/Medical Director at Nurix Therapeutics will primarily lead the development and execution of strategic Medical Affairs plans focused on hematology and oncology, particularly CLL. You'll support Clinical Development programs, forge essential relationships with external experts, and pave the way for research collaborations. Your role involves polishing scientific resources and training programs, guiding medical strategy development, and making insightful contributions to competitive intelligence analysis.

Ideal qualifications for the Scientific/Medical Director position at Nurix Therapeutics include an advanced degree such as MD, PharmD, PhD, or equivalent, alongside relevant experience in hematology or oncology settings. The candidate should possess 6+ years of experience in Medical Affairs or Clinical Development in the pharmaceutical or biotech industry, with a sound grasp of the regulatory landscape surrounding hematologic malignancies.

At Nurix Therapeutics, career development for the Scientific/Medical Director involves not just the opportunity to engage in high-impact projects but also continuous learning through collaborations with leading healthcare professionals and participation in scientific exchanges. We foster an environment where mentorship and collaboration help professionals grow their expertise while contributing to groundbreaking advancements in medicine.

Essential skills for the Scientific/Medical Director at Nurix Therapeutics include strong communication and leadership abilities, proven experience in generating effective medical affairs plans, and the capacity to work cross-functionally in a dynamic environment. A deep understanding of clinical research processes and the ability to engage with KOLs are critical for steering strategic medical and clinical directions.

The Scientific/Medical Director at Nurix Therapeutics can expect to travel approximately 30-40% of the time. This includes attending conferences, advisory board meetings, and engaging with stakeholders within the medical and scientific communities. Travel is essential for fostering partnerships and driving Nurix’s mission forward.

When discussing your experience in developing medical affairs plans, it's beneficial to provide specific examples of past plans you've created. Outline the strategies you utilized, the stakeholders you engaged with, and the outcomes of these plans. Highlight how you adapted your strategies based on clinical findings or feedback from experts to improve patient care.

In answering this question, emphasize the importance of open communication and mutual respect in cross-functional teamwork. Provide examples of successful collaborations you've participated in, detailing how you navigated challenges and aligned diverse perspectives to achieve common goals. This demonstrates your ability to work effectively in a fast-paced environment.

Showcase your commitment to continual learning by mentioning specific ways you stay updated, such as attending conferences, participating in webinars, reading industry journals, and engaging with thought leaders. Highlight how these efforts have positively influenced your work and contributed to the development of innovative therapies.

Discuss strategies like identifying key opinion leaders, understanding their research interests, and building relationships through scientific exchanges. Share examples where you've successfully fostered long-term partnerships, highlighting how these engagements contributed to your organization's strategic goals.

Talk about your approach to assessing unmet medical needs through literature reviews, discussions with clinical researchers, and insights gathered at conferences. Provide an example of how your findings have shaped the development of medical strategies at a previous position, showcasing your analytical skills and understanding of market dynamics.

In answering this, illustrate your time management and organizational skills. Detail how you prioritize tasks based on urgency and importance, and provide examples of how you have successfully managed multiple projects simultaneously by staying focused and organized under pressure.

When discussing your experience with regulatory submissions, be specific about the types of submissions you've prepared or contributed to. Detail the regulatory frameworks you've navigated, your role in the process, and how you ensured compliance, which can highlight your understanding of the regulatory environment for medicinal products.

Explain how data analysis has been integral to your decision-making process. Give examples of data-driven strategies you've implemented, how you interpreted data from clinical trials or market research, and the impact it has had on your work and the company’s strategy.

Provide a detailed account of a specific challenge you've encountered, how you approached it, and the ultimate resolution. This should showcase your problem-solving skills, adaptability, and how you maintained professionalism under pressure, reflecting your capabilities as a Scientific/Medical Director.

Discuss initiatives you've spearheaded, focusing on your goals and the methods employed to enhance Medical Education. Share the results of these initiatives and how they ultimately improved understanding among healthcare professionals and supported organizational objectives.