Assoc Director, Medical Affairs

Gilead Sciences•Foster City, CA

3d•$177,905 - $253,220•Remote

About The Position

The Associate Director US Medical Affairs, Patient Access and Quality of Care (PAQ) – Oncology will have responsibility for leading the development of Medical Affairs (MA) strategies and Plans of Action (POA) within a component of the Oncology Therapeutic Area (TA) for US payers and key accounts. This position will report to the Sr. Director, Strategy Lead of PAQ Oncology. The Associate Director Medical Affairs – PAQ Oncology will support the US launch planning and execution for novel pipeline products, as well as other products in the oncology portfolio.

Requirements

Bachelor's Degree and Ten Years’ Experience OR Masters' Degree and Eight Years’ Experience OR PhD and Two Years’ Experience

Nice To Haves

4+ years Medical Affairs (medical device/pharmaceutical industry), managed care, and HEOR experience, required.
Ideally including recent experience of a successful launch.
Demonstrated experience and expertise in health economics and outcomes research including writing research protocols, partnering to execute observational and economic research, and leveraging study design to support appropriate messages for strategic needs.
Advanced degree in life sciences in one or more of the following: MD, DO, PharmD, PhD
Significant health outcomes, research or medical affairs background in oncology.
Excellent strategic thinking skills, with demonstrated ability to successfully lead the ideation, development of a plan and move to action.
Possess a willingness and ability to work hands-on and with a sense of urgency, in a fast-paced, scientific, entrepreneurial environment.
Extensive knowledge of the US healthcare ecosystems, payer landscape and payer evidence requirements.
Existing contacts with payers, providers, advocates, institutions and/or hospitals strongly preferred.
Solid working knowledge of regulatory and compliance environment.
Effective organizational, project planning, and time management skills.
Strong sense of urgency and goal orientation.
Professional written and verbal communication skills with the ability to effectively present to and engage with a wide range of audiences.
Strong interpersonal skills including excellent verbal and written communication.
Proven ability for organizational partnership, strong teamwork, timely decision-making and the ability to work effectively in a matrix-environment within an evolving and fluid organization.
Computer proficiency in Excel, Word, PowerPoint, and Adobe®.
Ability to travel frequently (+/- 30%).
Display of Gilead Core Values: Integrity (Doing What’s Right), Teamwork (Working Together), Excellence (Being Your Best), Accountability (Taking Personal Responsibility), Inclusion (Encouraging Diversity).
People Leader Accountabilities: Create Inclusion, Develop Talent, Empower Teams.

Responsibilities

In collaboration with global and USMA TA, Managed Markets, Value and Access, Commercial and Government Affairs, develop Medical Affairs strategies and POA to ensure that PAQ is improving patient lives by aligning patient population needs, external stakeholder value drivers and Gilead portfolio and products.
Provide frequent internal and external input into the development of the US PAQ Strategic Plans as well as the Integrated Evidence Plan.
Identify and develop patient access strategy and research opportunities for US payers and key accounts ensuring alignment and inclusion of assigned MA activities, to support MA scientific objectives.
Act as scientific and execution lead for local US oncology PAQ studies and projects.
Understand PAQ OL needs, identify and communicate data gaps, and work collaboratively with research teams (Clinical Development, Medical Affairs Research, Value and Access Health Economic and Outcomes Research, Real-World Evidence) to actively address evidence needs throughout product lifecycle.
Accountable for providing PAQ strategic input into Publication Strategy.
Consistent with the scientific strategy, develop tools and resources to support successful implementation of the POA.
Work effectively with external vendor partners to complete required tools and resources.
Anticipate and coordinate necessary knowledge development for the PAQ team, ensure continuous and timely resources and training are provided to facilitate PAQ field team scientific knowledge and exchange.
Proactively share insights and evidence needs with the PAQ Strategy Lead.
In collaboration with PAQ field and cross-functional partners, contributes to strategy for real-world collaborative projects or studies and drives alignment with prioritized evidence needs / gaps.
Lead communication strategy with PAQ stakeholders, including leveraging the appropriate avenues for early scientific engagement and AMCP and preapproval dossier development.
In partnership with the FD’s, coordinate efforts for key PAQ conferences.
Assist with management of PAQ Medical Affairs Advisory Programs (MAAPs).
Develop and maintain positive professional relationships with PAQ thought leaders based on mutual respect and the sincere interest in sharing their perspective on medical therapies.
May be responsible for preparing and giving presentations for internal training and/or external audiences.
Collaborates effectively and in a compliant manner with colleagues in other functional areas throughout Gilead.