• The Principal Program Lead is a senior individual contributor responsible for leading the organization’s most complex, high-visibility strategic programs. • Working across business, technology, operations, and external partners, this role drives alignment, governance, execution, risk management, and delivery of initiatives that are critical to organizational success. • Principal Program Leads are deployed against the company’s highest-priority strategic initiatives and may move between programs over time based on business needs and portfolio priorities. • These leaders operate with significant autonomy and are accountable for driving successful outcomes across highly matrixed environments. • The initial assignment for this position will focus on technical delivery and operational readiness associated with major media facility construction and relocation initiatives. • Partnering closely with Global Real Estate, Engineering, Production Operations, Technology, Security, and external vendors, the Principal Program Lead will coordinate the successful delivery of all technology-related workstreams required to activate and transition new media facilities. • This role does not own facility design, construction, or real estate delivery. Instead, it serves as the strategic program leader responsible for integrating and coordinating the technology, operational readiness, and business transition activities necessary to support successful facility launches.

• Research and book flights, hotels, cruises, and vacation packages for clients. • Provide personalized recommendations and exceptional customer service. • Stay up to date on industry trends, deals, and travel requirements. • Market your travel services through social media and networking.

• At General Medicine, you will become part of a clinical community that is raising the standard for what virtual primary care can be — sharing our passion for making high-quality medicine accessible to everyone through telemedicine and intelligent technology. • We are seeking experienced physicians who thrive in fast-paced environments, lead with empathy and clinical rigor, and are passionate about delivering care that goes beyond a single interaction. • As a part-time virtual physician, you will practice as part of a broader care model that includes asynchronous and synchronous virtual care, coordination of labs and imaging, specialist e-consults, and referrals to in-person care when appropriate. • This is not high-volume, protocol-driven telehealth — clinicians remain involved in guiding patients through decisions and next steps, maintaining clinical ownership rather than handing care off after a single interaction. • The role is designed to fit naturally alongside an existing hospital, ED, or outpatient practice.

• Manage the product lifecycle from end of Phase II through launch to maximize commercial outcomes • Drive action throughout the organization to get prostate cancer therapeutics to market, and maximize their impact • Translate business and portfolio strategy into product strategy • Lead cross-functional planning for market launch in each territory where the asset marketing application is filed, approved, and registered for commercialization • Provide input and support to develop and on-board key vendors to manage high priority commercial projects assigned by the global product leadership team • Support and challenge overall product COGs, global forecasts, and NPV analysis • Collect and manage market research, market access and competitive intelligence relevant to the asset product • Evaluate product functionality and drive future product direction • Develop the global cross-functional plan including forward looking budget commitments and business case for the total addressable market • Provide market insights to internal and external stakeholders on the product and therapy area • Own the monthly product roadmap, including the plan, organization and execution for all activities for the asset product • Drive coordination and delivery through all functional relationships – clinical, clinical operations, regulatory affairs, manufacturing, quality and medical affairs • Complete and smooth transition from Phase II team to Phase III team to launch • Support and drive all activities related to Phase III trials • Drive end to end project management activities including communication, timelines, budget management and reporting • Monitor and act on risks and opportunities, including escalating as appropriate