Program Manager or Director, Cancer Vaccines

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    "jobTitle": "Program Manager or Director, Cancer Vaccines",
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    "description": "<p>The&nbsp;Foundation&nbsp;for&nbsp;the National Institute&nbsp;of Health&nbsp;(FNIH)&nbsp;is seeking&nbsp;a&nbsp;Program Manager&nbsp;or&nbsp;Director, with&nbsp;final&nbsp;level determined&nbsp;based on experience&nbsp;and&nbsp;leadership capabilities,&nbsp;to&nbsp;lead a high-profile, multi-sector national initiative to accelerate the development and clinical translation of next-generation cancer vaccines. This public&ndash;private partnership is designed to deliver near-term clinical proof-of-concept in high-risk, minimal residual disease (MRD+) cancers while building a scalable, long-term ecosystem for antigen discovery, vaccine development, manufacturing, and data-driven innovation.&nbsp;</p>\r\n\r\n<p>&nbsp;</p>\r\n\r\n<p>The&nbsp;Program Manager&nbsp;or&nbsp;Director&nbsp;will oversee a coordinated portfolio spanning rapid demonstration trials, parallel development of multiple antigen classes and vaccine platforms, scalable GMP manufacturing, harmonized immune monitoring, and a centralized data architecture enabling AI-driven antigen prediction. This position will report to the Senior Vice President of&nbsp;Translational&nbsp;Science&nbsp;within the&nbsp;Science Partnerships&nbsp;department&nbsp;(or their designated report)&nbsp;and&nbsp;is&nbsp;based&nbsp;at&nbsp;the&nbsp;FNIH&nbsp;offices&nbsp;located&nbsp;in&nbsp;North Bethesda, MD.&nbsp;</p>\r\n\r\n<p>&nbsp;</p>\r\n\r\n<p>This role requires a scientifically credible, operationally strong leader who can&nbsp;align&nbsp;partners&nbsp;across academia, biopharma, government, philanthropy,&nbsp;advocacy, and persons with live experience&nbsp;and translate complex science into coordinated execution. The&nbsp;Program Manager&nbsp;or&nbsp;Director will&nbsp;as a centralized facilitator&nbsp;for&nbsp;overall partnership development,&nbsp;vaccine&nbsp;candidate selection, adaptive clinical trial&nbsp;design and&nbsp;implementation,&nbsp;research project coordination,&nbsp;and funding strategy.&nbsp;</p>\r\n\r\n<p>Key Responsibilities&nbsp;</p>\r\n\r\n<p>Scientific &amp; Program Leadership&nbsp;&amp; Portfolio Management&nbsp;</p>\r\n\r\n<ul>\r\n\t<li>\r\n\t<p>Lead the overall scientific and operational&nbsp;partnership&nbsp;strategy for the Cancer Vaccines Initiative&nbsp;and eventually other projects&nbsp;</p>\r\n\t</li>\r\n</ul>\r\n\r\n<ul>\r\n\t<li>\r\n\t<p>Facilitate the definition&nbsp;and prioritization of&nbsp;high-impact use cases, including rapid &ldquo;quick win&rdquo; demonstration trials in MRD+ cancer settings&nbsp;</p>\r\n\t</li>\r\n</ul>\r\n\r\n<ul>\r\n\t<li>\r\n\t<p>Ensure alignment of&nbsp;the groups working on&nbsp;antigen discovery,&nbsp;preclinical development,&nbsp;vaccine platforms,&nbsp;manufacturing,&nbsp;and clinical&nbsp;design and execution&nbsp;</p>\r\n\t</li>\r\n</ul>\r\n\r\n<ul>\r\n\t<li>\r\n\t<p>Lead collaborative processes to&nbsp;identify&nbsp;and prioritize candidate antigens, vaccine constructs, and combination strategies&nbsp;</p>\r\n\t</li>\r\n</ul>\r\n\r\n<ul>\r\n\t<li>\r\n\t<p>Establish criteria for advancement, down-selection, and portfolio evolution&nbsp;</p>\r\n\t</li>\r\n</ul>\r\n\r\n<ul>\r\n\t<li>\r\n\t<p>Represent the initiative in scientific, clinical, and policy forums&nbsp;</p>\r\n\t</li>\r\n</ul>\r\n\r\n<ul>\r\n\t<li>\r\n\t<p>Contribute to publications, presentations, and strategic communications&nbsp;</p>\r\n\t</li>\r\n</ul>\r\n\r\n<p>Clinical Trial Strategy &amp; Execution&nbsp;</p>\r\n\r\n<ul>\r\n\t<li>\r\n\t<p>Oversee design and execution of&nbsp;adaptive, efficient clinical trials focused on early signals of efficacy and immune response&nbsp;</p>\r\n\t</li>\r\n</ul>\r\n\r\n<ul>\r\n\t<li>\r\n\t<p>Ensure rigorous trial design, site&nbsp;selection, and execution across multiple institutions&nbsp;</p>\r\n\t</li>\r\n</ul>\r\n\r\n<ul>\r\n\t<li>\r\n\t<p>Integrate biomarkers and immune monitoring into trial design and analysis&nbsp;</p>\r\n\t</li>\r\n</ul>\r\n\r\n<ul>\r\n\t<li>\r\n\t<p>Drive speed, quality, and comparability across trials&nbsp;</p>\r\n\t</li>\r\n</ul>\r\n\r\n<p>Manufacturing &amp; Immune Monitoring Infrastructure&nbsp;</p>\r\n\r\n<ul>\r\n\t<li>\r\n\t<p>Oversee development of scalable GMP manufacturing approaches across platforms&nbsp;</p>\r\n\t</li>\r\n</ul>\r\n\r\n<ul>\r\n\t<li>\r\n\t<p>Ensure harmonization of immune monitoring assays and endpoints across studies&nbsp;</p>\r\n\t</li>\r\n</ul>\r\n\r\n<p>Data &amp; AI-Enabled Innovation&nbsp;</p>\r\n\r\n<ul>\r\n\t<li>\r\n\t<p>Partner with data science leadership to build and&nbsp;utilize&nbsp;centralized data architecture supporting the initiative&nbsp;</p>\r\n\t</li>\r\n</ul>\r\n\r\n<ul>\r\n\t<li>\r\n\t<p>Enable integration of clinical, immunologic, and molecular data to inform antigen prediction and vaccine design&nbsp;</p>\r\n\t</li>\r\n</ul>\r\n\r\n<ul>\r\n\t<li>\r\n\t<p>Support AI-driven approaches to&nbsp;optimize&nbsp;candidate&nbsp;selection&nbsp;and trial learning&nbsp;</p>\r\n\t</li>\r\n</ul>\r\n\r\n<p>Regulatory Strategy &amp; Engagement&nbsp;</p>\r\n\r\n<ul>\r\n\t<li>\r\n\t<p>Collaborate with regulatory agencies to&nbsp;align&nbsp;innovative trial designs, endpoints, and biomarker strategies&nbsp;</p>\r\n\t</li>\r\n</ul>\r\n\r\n<ul>\r\n\t<li>\r\n\t<p>Ensure programs are designed to support future regulatory pathways and potential approval&nbsp;</p>\r\n\t</li>\r\n</ul>\r\n\r\n<ul>\r\n\t<li>\r\n\t<p>Help to&nbsp;facilitate&nbsp;regulatory submissions and advice interactions,&nbsp;as needed&nbsp;</p>\r\n\t</li>\r\n</ul>\r\n\r\n<p>Partnership Development &amp;&nbsp;Partner&nbsp;Engagement&nbsp;</p>\r\n\r\n<ul>\r\n\t<li>\r\n\t<p>Lead engagement with biopharmaceutical companies, academic investigators, technology partners,&nbsp;philanthropists, advocacy groups, and persons with lived experience&nbsp;</p>\r\n\t</li>\r\n</ul>\r\n\r\n<ul>\r\n\t<li>\r\n\t<p>Build and sustain a collaborative ecosystem aligned around shared scientific and translational goals, including philanthropy and government&nbsp;</p>\r\n\t</li>\r\n</ul>\r\n\r\n<ul>\r\n\t<li>\r\n\t<p>Partner with&nbsp;Strategic Alliances and Advancement&nbsp;to secure and align funding to support initiative goals&nbsp;</p>\r\n\t</li>\r\n</ul>\r\n\r\n<ul>\r\n\t<li>\r\n\t<p>Articulate the value proposition and&nbsp;impact&nbsp;of the initiative to diverse funders&nbsp;</p>\r\n\t</li>\r\n</ul>\r\n\r\n<p>Program Governance &amp; Execution&nbsp;</p>\r\n\r\n<ul>\r\n\t<li>\r\n\t<p>Establish and lead governance structures, including&nbsp;executive and&nbsp;steering committees and scientific advisory groups&nbsp;</p>\r\n\t</li>\r\n</ul>\r\n\r\n<ul>\r\n\t<li>\r\n\t<p>Oversee timelines, milestones, budgets, and deliverables across all program components&nbsp;</p>\r\n\t</li>\r\n</ul>\r\n\r\n<ul>\r\n\t<li>\r\n\t<p>Ensure transparency, accountability, and effective decision-making across&nbsp;all partners and any relevant external&nbsp;organizations&nbsp;</p>\r\n\t</li>\r\n</ul>\r\n",
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Execution&nbsp;\\r\\n\\r\\n\\r\\n\\t\\r\\n\\tOversee design and execution of&nbsp;adaptive, efficient clinical trials focused on early signals of efficacy and immune response&nbsp;\\r\\n\\t\\r\\n\\r\\n\\r\\n\\r\\n\\t\\r\\n\\tEnsure rigorous trial design, site&nbsp;selection, and execution across multiple institutions&nbsp;\\r\\n\\t\\r\\n\\r\\n\\r\\n\\r\\n\\t\\r\\n\\tIntegrate biomarkers and immune monitoring into trial design and analysis&nbsp;\\r\\n\\t\\r\\n\\r\\n\\r\\n\\r\\n\\t\\r\\n\\tDrive speed, quality, and comparability across trials&nbsp;\\r\\n\\t\\r\\n\\r\\n\\r\\nManufacturing &amp; Immune Monitoring Infrastructure&nbsp;\\r\\n\\r\\n\\r\\n\\t\\r\\n\\tOversee development of scalable GMP manufacturing approaches across platforms&nbsp;\\r\\n\\t\\r\\n\\r\\n\\r\\n\\r\\n\\t\\r\\n\\tEnsure harmonization of immune monitoring assays and endpoints across studies&nbsp;\\r\\n\\t\\r\\n\\r\\n\\r\\nData &amp; AI-Enabled Innovation&nbsp;\\r\\n\\r\\n\\r\\n\\t\\r\\n\\tPartner with data science leadership to build and&nbsp;utilize&nbsp;centralized data architecture supporting the initiative&nbsp;\\r\\n\\t\\r\\n\\r\\n\\r\\n\\r\\n\\t\\r\\n\\tEnable integration of clinical, immunologic, and molecular data to inform antigen prediction and vaccine design&nbsp;\\r\\n\\t\\r\\n\\r\\n\\r\\n\\r\\n\\t\\r\\n\\tSupport AI-driven approaches to&nbsp;optimize&nbsp;candidate&nbsp;selection&nbsp;and trial learning&nbsp;\\r\\n\\t\\r\\n\\r\\n\\r\\nRegulatory Strategy &amp; Engagement&nbsp;\\r\\n\\r\\n\\r\\n\\t\\r\\n\\tCollaborate with regulatory agencies to&nbsp;align&nbsp;innovative trial designs, endpoints, and biomarker strategies&nbsp;\\r\\n\\t\\r\\n\\r\\n\\r\\n\\r\\n\\t\\r\\n\\tEnsure programs are designed to support future regulatory pathways and potential approval&nbsp;\\r\\n\\t\\r\\n\\r\\n\\r\\n\\r\\n\\t\\r\\n\\tHelp to&nbsp;facilitate&nbsp;regulatory submissions and advice interactions,&nbsp;as needed&nbsp;\\r\\n\\t\\r\\n\\r\\n\\r\\nPartnership Development &amp;&nbsp;Partner&nbsp;Engagement&nbsp;\\r\\n\\r\\n\\r\\n\\t\\r\\n\\tLead engagement with biopharmaceutical companies, academic investigators, technology partners,&nbsp;philanthropists, advocacy groups, and persons with lived experience&nbsp;\\r\\n\\t\\r\\n\\r\\n\\r\\n\\r\\n\\t\\r\\n\\tBuild and sustain a collaborative ecosystem aligned around shared scientific and translational goals, including philanthropy and government&nbsp;\\r\\n\\t\\r\\n\\r\\n\\r\\n\\r\\n\\t\\r\\n\\tPartner with&nbsp;Strategic Alliances and Advancement&nbsp;to secure and align funding to support initiative goals&nbsp;\\r\\n\\t\\r\\n\\r\\n\\r\\n\\r\\n\\t\\r\\n\\tArticulate the value proposition and&nbsp;impact&nbsp;of the initiative to diverse funders&nbsp;\\r\\n\\t\\r\\n\\r\\n\\r\\nProgram Governance &amp; Execution&nbsp;\\r\\n\\r\\n\\r\\n\\t\\r\\n\\tEstablish and lead governance structures, including&nbsp;executive and&nbsp;steering committees and scientific advisory groups&nbsp;\\r\\n\\t\\r\\n\\r\\n\\r\\n\\r\\n\\t\\r\\n\\tOversee timelines, milestones, budgets, and deliverables across all program components&nbsp;\\r\\n\\t\\r\\n\\r\\n\\r\\n\\r\\n\\t\\r\\n\\tEnsure transparency, accountability, and effective decision-making across&nbsp;all partners and any relevant external&nbsp;organizations&nbsp;\\r\\n\\t\\r\\n\\r\\nQualificationsRequired&nbsp;\\r\\n\\r\\n\\r\\n\\t\\r\\n\\tMD, PhD, or equivalent in oncology, immunology, or related biomedical field&nbsp;&nbsp;\\r\\n\\t\\r\\n\\r\\n\\r\\n\\r\\n\\t\\r\\n\\tProgram Manager candidates should have approximately 7+ years of relevant experience in oncology drug development, cancer immunotherapy, or vaccine development, while Director&nbsp;level&nbsp;candidates should have 10+ years of progressively responsible experience in these areas.&nbsp;\\r\\n\\t\\r\\n\\r\\n\\r\\n\\r\\n\\t\\r\\n\\tStrong understanding of translational science across discovery, preclinical, and clinical domains, including&nbsp;clinical trial design and execution, including multi-site studies&nbsp;\\r\\n\\t\\r\\n\\r\\n\\r\\n\\r\\n\\t\\r\\n\\tProven ability to lead complex, multi-institutional or public&ndash;private partnerships&nbsp;\\r\\n\\t\\r\\n\\r\\n\\r\\nPreferred&nbsp;\\r\\n\\r\\n\\r\\n\\t\\r\\n\\tExperience interacting with regulatory agencies (e.g., FDA, EMA)&nbsp;\\r\\n\\t\\r\\n\\r\\n\\r\\n\\r\\n\\t\\r\\n\\tExperience with cancer vaccines, immuno-oncology, or antigen discovery platforms&nbsp;\\r\\n\\t\\r\\n\\r\\n\\r\\n\\r\\n\\t\\r\\n\\tFamiliarity with GMP manufacturing and immune monitoring technologies&nbsp;\\r\\n\\t\\r\\n\\r\\n\\r\\n\\r\\n\\t\\r\\n\\tExperience with adaptive trial designs and biomarker-driven development&nbsp;\\r\\n\\t\\r\\n\\r\\n\\r\\n\\r\\n\\t\\r\\n\\tTrack record&nbsp;of high-impact&nbsp;team&nbsp;leadership&nbsp;\\r\\n\\t\\r\\n\\r\\n\\r\\nThis is a hybrid position and requires regular visits to FNIH headquarters in Bethesda, MD. This&nbsp;position&nbsp;may&nbsp;also&nbsp;require&nbsp;occasional travel for meetings,&nbsp;conferences&nbsp;and any&nbsp;other&nbsp;relevant engagements.&nbsp;&nbsp;\\r\\n\\r\\n&nbsp;\\r\\n\\r\\nAt FNIH we are committed to living our core values every day. If you are excited about this role and the work of the Foundation, but your experience doesn&rsquo;t align perfectly with all the qualifications in the job description, we encourage you to apply nonetheless. You may be just the right candidate for this or other roles at FNIH. &nbsp;\\r\\n\",\"responsibilities\":\"The&nbsp;Foundation&nbsp;for&nbsp;the National Institute&nbsp;of Health&nbsp;(FNIH)&nbsp;is seeking&nbsp;a&nbsp;Program Manager&nbsp;or&nbsp;Director, with&nbsp;final&nbsp;level determined&nbsp;based on experience&nbsp;and&nbsp;leadership capabilities,&nbsp;to&nbsp;lead a high-profile, multi-sector national initiative to accelerate the development and clinical translation of next-generation cancer vaccines. This public&ndash;private partnership is designed to deliver near-term clinical proof-of-concept in high-risk, minimal residual disease (MRD+) cancers while building a scalable, long-term ecosystem for antigen discovery, vaccine development, manufacturing, and data-driven innovation.&nbsp;\\r\\n\\r\\n&nbsp;\\r\\n\\r\\nThe&nbsp;Program Manager&nbsp;or&nbsp;Director&nbsp;will oversee a coordinated portfolio spanning rapid demonstration trials, parallel development of multiple antigen classes and vaccine platforms, scalable GMP manufacturing, harmonized immune monitoring, and a centralized data architecture enabling AI-driven antigen prediction. This position will report to the Senior Vice President of&nbsp;Translational&nbsp;Science&nbsp;within the&nbsp;Science Partnerships&nbsp;department&nbsp;(or their designated report)&nbsp;and&nbsp;is&nbsp;based&nbsp;at&nbsp;the&nbsp;FNIH&nbsp;offices&nbsp;located&nbsp;in&nbsp;North Bethesda, MD.&nbsp;\\r\\n\\r\\n&nbsp;\\r\\n\\r\\nThis role requires a scientifically credible, operationally strong leader who can&nbsp;align&nbsp;partners&nbsp;across academia, biopharma, government, philanthropy,&nbsp;advocacy, and persons with live experience&nbsp;and translate complex science into coordinated execution. The&nbsp;Program Manager&nbsp;or&nbsp;Director will&nbsp;as a centralized facilitator&nbsp;for&nbsp;overall partnership development,&nbsp;vaccine&nbsp;candidate selection, adaptive clinical trial&nbsp;design and&nbsp;implementation,&nbsp;research project coordination,&nbsp;and funding strategy.&nbsp;\\r\\n\\r\\nKey Responsibilities&nbsp;\\r\\n\\r\\nScientific &amp; Program Leadership&nbsp;&amp; Portfolio Management&nbsp;\\r\\n\\r\\n\\r\\n\\t\\r\\n\\tLead the overall scientific and operational&nbsp;partnership&nbsp;strategy for the Cancer Vaccines Initiative&nbsp;and eventually other projects&nbsp;\\r\\n\\t\\r\\n\\r\\n\\r\\n\\r\\n\\t\\r\\n\\tFacilitate the definition&nbsp;and prioritization of&nbsp;high-impact use cases, including rapid &ldquo;quick win&rdquo; demonstration trials in MRD+ cancer settings&nbsp;\\r\\n\\t\\r\\n\\r\\n\\r\\n\\r\\n\\t\\r\\n\\tEnsure alignment of&nbsp;the groups working on&nbsp;antigen discovery,&nbsp;preclinical development,&nbsp;vaccine platforms,&nbsp;manufacturing,&nbsp;and clinical&nbsp;design and execution&nbsp;\\r\\n\\t\\r\\n\\r\\n\\r\\n\\r\\n\\t\\r\\n\\tLead collaborative processes to&nbsp;identify&nbsp;and prioritize candidate antigens, vaccine constructs, and combination strategies&nbsp;\\r\\n\\t\\r\\n\\r\\n\\r\\n\\r\\n\\t\\r\\n\\tEstablish criteria for advancement, down-selection, and portfolio evolution&nbsp;\\r\\n\\t\\r\\n\\r\\n\\r\\n\\r\\n\\t\\r\\n\\tRepresent the initiative in scientific, clinical, and policy forums&nbsp;\\r\\n\\t\\r\\n\\r\\n\\r\\n\\r\\n\\t\\r\\n\\tContribute to publications, presentations, and strategic communications&nbsp;\\r\\n\\t\\r\\n\\r\\n\\r\\nClinical Trial Strategy &amp; Execution&nbsp;\\r\\n\\r\\n\\r\\n\\t\\r\\n\\tOversee design and execution of&nbsp;adaptive, efficient clinical trials focused on early signals of efficacy and immune response&nbsp;\\r\\n\\t\\r\\n\\r\\n\\r\\n\\r\\n\\t\\r\\n\\tEnsure rigorous trial design, site&nbsp;selection, and execution across multiple institutions&nbsp;\\r\\n\\t\\r\\n\\r\\n\\r\\n\\r\\n\\t\\r\\n\\tIntegrate biomarkers and immune monitoring into trial design and analysis&nbsp;\\r\\n\\t\\r\\n\\r\\n\\r\\n\\r\\n\\t\\r\\n\\tDrive speed, quality, and comparability across trials&nbsp;\\r\\n\\t\\r\\n\\r\\n\\r\\nManufacturing &amp; Immune Monitoring Infrastructure&nbsp;\\r\\n\\r\\n\\r\\n\\t\\r\\n\\tOversee development of scalable GMP manufacturing approaches across platforms&nbsp;\\r\\n\\t\\r\\n\\r\\n\\r\\n\\r\\n\\t\\r\\n\\tEnsure harmonization of immune monitoring assays and endpoints across studies&nbsp;\\r\\n\\t\\r\\n\\r\\n\\r\\nData &amp; AI-Enabled Innovation&nbsp;\\r\\n\\r\\n\\r\\n\\t\\r\\n\\tPartner with data science leadership to build and&nbsp;utilize&nbsp;centralized data architecture supporting the initiative&nbsp;\\r\\n\\t\\r\\n\\r\\n\\r\\n\\r\\n\\t\\r\\n\\tEnable integration of clinical, immunologic, and molecular data to inform antigen prediction and vaccine design&nbsp;\\r\\n\\t\\r\\n\\r\\n\\r\\n\\r\\n\\t\\r\\n\\tSupport AI-driven approaches to&nbsp;optimize&nbsp;candidate&nbsp;selection&nbsp;and trial learning&nbsp;\\r\\n\\t\\r\\n\\r\\n\\r\\nRegulatory Strategy &amp; Engagement&nbsp;\\r\\n\\r\\n\\r\\n\\t\\r\\n\\tCollaborate with regulatory agencies to&nbsp;align&nbsp;innovative trial designs, endpoints, and biomarker strategies&nbsp;\\r\\n\\t\\r\\n\\r\\n\\r\\n\\r\\n\\t\\r\\n\\tEnsure programs are designed to support future regulatory pathways and potential approval&nbsp;\\r\\n\\t\\r\\n\\r\\n\\r\\n\\r\\n\\t\\r\\n\\tHelp to&nbsp;facilitate&nbsp;regulatory submissions and advice interactions,&nbsp;as needed&nbsp;\\r\\n\\t\\r\\n\\r\\n\\r\\nPartnership Development &amp;&nbsp;Partner&nbsp;Engagement&nbsp;\\r\\n\\r\\n\\r\\n\\t\\r\\n\\tLead engagement with biopharmaceutical companies, academic investigators, technology partners,&nbsp;philanthropists, advocacy groups, and persons with lived experience&nbsp;\\r\\n\\t\\r\\n\\r\\n\\r\\n\\r\\n\\t\\r\\n\\tBuild and sustain a collaborative ecosystem aligned around shared scientific and translational goals, including philanthropy and government&nbsp;\\r\\n\\t\\r\\n\\r\\n\\r\\n\\r\\n\\t\\r\\n\\tPartner with&nbsp;Strategic Alliances and Advancement&nbsp;to secure and align funding to support initiative goals&nbsp;\\r\\n\\t\\r\\n\\r\\n\\r\\n\\r\\n\\t\\r\\n\\tArticulate the value proposition and&nbsp;impact&nbsp;of the initiative to diverse funders&nbsp;\\r\\n\\t\\r\\n\\r\\n\\r\\nProgram Governance &amp; Execution&nbsp;\\r\\n\\r\\n\\r\\n\\t\\r\\n\\tEstablish and lead governance structures, including&nbsp;executive and&nbsp;steering committees and scientific advisory groups&nbsp;\\r\\n\\t\\r\\n\\r\\n\\r\\n\\r\\n\\t\\r\\n\\tOversee timelines, milestones, budgets, and deliverables across all program components&nbsp;\\r\\n\\t\\r\\n\\r\\n\\r\\n\\r\\n\\t\\r\\n\\tEnsure transparency, accountability, and effective decision-making across&nbsp;all partners and any relevant external&nbsp;organizations&nbsp;\\r\\n\\t\\r\\n\\r\\n\",\"employmentType\":\"FULL_TIME\",\"hiringOrganization\":{\"@type\":\"Organization\",\"name\":\"Foundation for the National Institutes of Health (FNIH)\",\"logo\":\"https://www.paycomonline.net/v4/ats/web.php/application/style/logo?clientkey=BFFEFEF0151216F871FDA32CD359CE3F\"},\"jobLocation\":{\"@type\":\"Place\",\"address\":{\"streetAddress\":\"11400 Rockville Pike\",\"addressLocality\":\"North Bethesda\",\"addressRegion\":\"MD\",\"postalCode\":20852,\"addressCountry\":\"USA\"}},\"qualifications\":\"Required&nbsp;\\r\\n\\r\\n\\r\\n\\t\\r\\n\\tMD, PhD, or equivalent in oncology, immunology, or related biomedical field&nbsp;&nbsp;\\r\\n\\t\\r\\n\\r\\n\\r\\n\\r\\n\\t\\r\\n\\tProgram Manager candidates should have approximately 7+ years of relevant experience in oncology drug development, cancer immunotherapy, or vaccine development, while Director&nbsp;level&nbsp;candidates should have 10+ years of progressively responsible experience in these areas.&nbsp;\\r\\n\\t\\r\\n\\r\\n\\r\\n\\r\\n\\t\\r\\n\\tStrong understanding of translational science across discovery, preclinical, and clinical domains, including&nbsp;clinical trial design and execution, including multi-site studies&nbsp;\\r\\n\\t\\r\\n\\r\\n\\r\\n\\r\\n\\t\\r\\n\\tProven ability to lead complex, multi-institutional or public&ndash;private partnerships&nbsp;\\r\\n\\t\\r\\n\\r\\n\\r\\nPreferred&nbsp;\\r\\n\\r\\n\\r\\n\\t\\r\\n\\tExperience interacting with regulatory agencies (e.g., FDA, EMA)&nbsp;\\r\\n\\t\\r\\n\\r\\n\\r\\n\\r\\n\\t\\r\\n\\tExperience with cancer vaccines, immuno-oncology, or antigen discovery platforms&nbsp;\\r\\n\\t\\r\\n\\r\\n\\r\\n\\r\\n\\t\\r\\n\\tFamiliarity with GMP manufacturing and immune monitoring technologies&nbsp;\\r\\n\\t\\r\\n\\r\\n\\r\\n\\r\\n\\t\\r\\n\\tExperience with adaptive trial designs and biomarker-driven development&nbsp;\\r\\n\\t\\r\\n\\r\\n\\r\\n\\r\\n\\t\\r\\n\\tTrack record&nbsp;of high-impact&nbsp;team&nbsp;leadership&nbsp;\\r\\n\\t\\r\\n\\r\\n\\r\\nThis is a hybrid position and requires regular visits to FNIH headquarters in Bethesda, MD. This&nbsp;position&nbsp;may&nbsp;also&nbsp;require&nbsp;occasional travel for meetings,&nbsp;conferences&nbsp;and any&nbsp;other&nbsp;relevant engagements.&nbsp;&nbsp;\\r\\n\\r\\n&nbsp;\\r\\n\\r\\nAt FNIH we are committed to living our core values every day. If you are excited about this role and the work of the Foundation, but your experience doesn&rsquo;t align perfectly with all the qualifications in the job description, we encourage you to apply nonetheless. You may be just the right candidate for this or other roles at FNIH. &nbsp;\\r\\n\",\"experienceRequirements\":\"Required&nbsp;\\r\\n\\r\\n\\r\\n\\t\\r\\n\\tMD, PhD, or equivalent in oncology, immunology, or related biomedical field&nbsp;&nbsp;\\r\\n\\t\\r\\n\\r\\n\\r\\n\\r\\n\\t\\r\\n\\tProgram Manager candidates should have approximately 7+ years of relevant experience in oncology drug development, cancer immunotherapy, or vaccine development, while Director&nbsp;level&nbsp;candidates should have 10+ years of progressively responsible experience in these areas.&nbsp;\\r\\n\\t\\r\\n\\r\\n\\r\\n\\r\\n\\t\\r\\n\\tStrong understanding of translational science across discovery, preclinical, and clinical domains, including&nbsp;clinical trial design and execution, including multi-site studies&nbsp;\\r\\n\\t\\r\\n\\r\\n\\r\\n\\r\\n\\t\\r\\n\\tProven ability to lead complex, multi-institutional or public&ndash;private partnerships&nbsp;\\r\\n\\t\\r\\n\\r\\n\\r\\nPreferred&nbsp;\\r\\n\\r\\n\\r\\n\\t\\r\\n\\tExperience interacting with regulatory agencies (e.g., FDA, EMA)&nbsp;\\r\\n\\t\\r\\n\\r\\n\\r\\n\\r\\n\\t\\r\\n\\tExperience with cancer vaccines, immuno-oncology, or antigen discovery platforms&nbsp;\\r\\n\\t\\r\\n\\r\\n\\r\\n\\r\\n\\t\\r\\n\\tFamiliarity with GMP manufacturing and immune monitoring technologies&nbsp;\\r\\n\\t\\r\\n\\r\\n\\r\\n\\r\\n\\t\\r\\n\\tExperience with adaptive trial designs and biomarker-driven development&nbsp;\\r\\n\\t\\r\\n\\r\\n\\r\\n\\r\\n\\t\\r\\n\\tTrack record&nbsp;of high-impact&nbsp;team&nbsp;leadership&nbsp;\\r\\n\\t\\r\\n\\r\\n\\r\\nThis is a hybrid position and requires regular visits to FNIH headquarters in Bethesda, MD. 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