Medical Director, Small Cell Lung Cancer

AstraZeneca • Gaithersburg, MD

1d • $193,000 - $289,000 • Hybrid

About The Position

The Medical Director, Small Cell Lung Cancer is a pivotal role within the US Oncology Medical Affairs organization. Reporting directly to the Medical Head, this position is accountable for driving medical plans for specific or multiple indications within a designated disease area. AstraZeneca is a global, science-led, patient-focused biopharmaceutical company. We focus on discovering, developing and commercialising prescription medicines for some of the world’s most serious diseases. At AstraZeneca, we’re dedicated to being a Great Place to Work. Where you are empowered to push the boundaries of science, challenge convention and unleash your entrepreneurial spirit. To embrace differences and take bold actions to drive the change needed to meet global healthcare and sustainability challenges. There is no better place to make a difference in medicine, patients, and society. An inclusive culture where you will connect different thinking to generate new and valuable opportunities. Where you will find a commitment to lifelong learning, growth and development for all. Our Inclusion & Diversity (I&D) mission is to create an inclusive and equitable environment where people belong, using the power of our diversity to push the boundaries of science to deliver life-changing medicines to patients. Inclusion and diversity are fundamental to the success of our company, because innovation requires breakthrough ideas that only come from a diverse workforce empowered to challenge conventional thinking. We’re curious about science and the advancement of knowledge. We find creative ways to approach new challenges. We’re driven to make the right choices and be accountable for our actions. As an organisation centred around what makes us human, we put a big focus on people. Across our business, we want colleagues to wake up excited about their day at the office, in the field, or in the lab. Along with our purpose to bring life-changing medicines to people across the globe, we have a promise to you: to help you realise the full breadth of your potential. Here, you’ll do work that has the potential to change your life and improve countless others. And, together with your team, you’ll shape a culture that unites and inspires us every day. This is your life at AstraZeneca.

Requirements

• Advanced Medical/Scientific Degree (Masters minimum; advanced degree strongly preferred in a scientific background)
• 3+ years of Medical Affairs experience in the pharmaceutical industry (including at least 1 year of headquarter experience)
• Prior experience in pharmaceutical industry headquarters Medical Affairs functions
• Validated experience in relationship and collaborator management with the 3 P's (Payers, Providers, and Patients)
• Demonstrated project and relationship management experience
• Experience with evidence generation and clinical trial methodology
• Foundation knowledge in business operations and strategy
• Foundation knowledge in financial management and budget tracking
• Specialist-level experience working effectively in matrix organizations

Nice To Haves

• PharmD, MD, PhD
• Understanding of technical, regulatory, policy, and real-world evidence generation dimensions
• Direct experience leading departmental or project budgets
• Experience developing and delivering country-level medical affairs plans

Responsibilities

• Coordinate development of the integrated Medical Affairs Plan (iMAP), complete key projects, and track budget spend
• Support Launch Readiness Reviews (LRR) by coordinating and supervising pre-launch activities, ensuring timely execution of endorsed LRR plans
• Synthesize field insights into practical tactics, connect with business collaborators, and modify plans as necessary
• Complete all Medical Affairs Leadership Team (MALT) initiatives as requested
• Support quarterly iMAP reviews at the Core Medical Team (CMT) in collaboration with the Medical Lead
• Support the Promotional Materials Review Team (PMRT) by reviewing derivative content for scientific accuracy and compliance
• Support the Medical Lead on the CMT
• Implement and supervise KEE engagement plans with follow-up to improve engagement and impact
• Independently set meeting objectives, develop discussion guides, and lead communications with vendors to execute effective Advisory Boards
• Plan congress activities, gather insights, handling communications, and partner with Field leadership to ensure effective pull-through at events
• Conduct evidence publication reviews and participate in Medical Education Grants Office (MEGO) selection processes
• Complete Medical projects while staying within scope and budget
• Work closely with Medical Affairs colleagues on research alliance initiatives, capability development programs, and tools/technology initiatives
• Adhere to all ethical and compliance standards as determined by the organization and/or market regulations

Benefits

• short-term incentive bonus opportunity
• equity-based long-term incentive program
• retirement contribution
• commission payment eligibility
• qualified retirement program [401(k) plan]
• paid vacation and holidays
• paid leaves
• health benefits including medical, prescription drug, dental, and vision coverage

What This Job Offers

• Job Type: Full-time
• Career Level: Senior