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American Society of Clinical Oncology (ASCO) · 1 week ago

Associate Director, Science and Research Policy

Alexandria, VA

Full-time

Hybrid

Senior Level, Lead/Staff, Director/Executive

7+ years exp

The American Society of Clinical Oncology (ASCO) is committed to conquering cancer through research, education, and promotion of high-quality care. They are seeking an experienced Associate Director, Science and Research Policy to lead efforts at the intersection of science, health, and federal policy, serving as a trusted advisor to ASCO leadership and ensuring the Society’s policy priorities advance cancer research and care.

Health CareNon ProfitOncology

Culture & Values

Responsibilities

Function as a content and subject matter expert regarding policies and regulatory actions that impact clinical research and cancer care delivery, e.g., drug- and biomarker approval, trial design, diagnostics, and drug shortages

Monitor, analyze, and project impact of proposed regulations or other administrative actions; and provide input on proposed legislation and its impact on cancer care and research, as appropriate

Lead ASCO’s formal response to regulatory issues, including drafting of comments. Support development of ASCO advocacy materials, testimony, and other materials as appropriate

Identify and pursue opportunities to build and maintain relationships with Agency staff and relevant external stakeholders to work collaboratively and raise ASCO’s visibility on positions related to cancer research and care

Prepare succinct and substantive written and oral regulatory updates for membership communications and serve as a resource for ASCO members on regulatory issues. Present updates as appropriate to ASCO committees, state societies, and other organizations as appropriate

Provide strategic leadership to the Government Relations Committee and other ASCO committees and task forces on regulatory affairs, including impact on political positioning, and advocacy strategies. Represent ASCO priorities and perspectives in external coalitions, on task forces, with federal agencies, and on Capitol Hill, when needed

Participate and contribute to strategic planning including identifying emerging policy areas needed for ASCO action

Qualification

Regulatory affairsLegislative processCancer research knowledgePublic policyProject managementAnalytical skillsCommunication skillsInterpersonal skillsTeam collaborationLeadership abilities

Required

Bachelor's degree in public policy, health- or science-related discipline or equivalent years of experience

7+ years' experience with the regulatory and/or legislative process, preferably as Agency or Congressional staff, consultant, or in a related capacity, with a focus on healthcare issues

Experience in regulatory and legislative affairs and a strong knowledge of lead scientific research agencies at the federal level (e.g., NIH/NCI, FDA, CDC, ARPA-H, and related subagencies and organizations)

Demonstrated knowledge of laws, rules, regulations, and policies affecting cancer research, including use of common federal tracking systems and web resources

Outstanding communication skills, including written and presentation skills, with the ability to effectively interact with all levels of internal organization and external stakeholders

The ability to work effectively in a collaborative, team environment while also being self-directed

Excellent organization and project management skills with high attention to detail

Strong leadership and influencing abilities; politically astute

Strong interpersonal skills with ability to build and maintain relationships internally and externally with agency leaders and their staff

Demonstrated integrity and evidence-based, informed decision making

Ability to analyze policy, regulatory, and guidance changes and to communicate their separate and combined impact to ASCO members and leadership

Outstanding time management skills with a proven ability to meet deadlines, prioritize workload, and multi-task

Preferred

Advanced degree preferable, especially in health-research or science-related field

Demonstrated knowledge of regulatory issues impacting the cancer research enterprise, including but not limited to clinical trials, drug development, and funding

Previous experience working for a cancer non-profit or association or member organization