Home › Companies › Uscareers Lumanity Icims Com › Vice President, Regulatory Strategy
Vice President, Regulatory Strategy
Uscareers Lumanity Icims Com · Remote, UNAVAILABLE, US · Remote · Active · iCIMS
Job facts
| Field | Value |
|---|---|
| Company | Uscareers Lumanity Icims Com |
| Title | Vice President, Regulatory Strategy |
| Normalized title | - |
| Department / team | Clinical and Regulatory |
| Location | UNAVAILABLE, United States |
| Work model | Remote / Remote |
| Employment type | OTHER |
| Salary | - |
| Status | active |
| ATS provider | iCIMS |
| Posted / first seen | 2026-05-08 / 2026-05-31 |
| Changed / last seen | 2026-06-01 / 2026-06-06 |
Related slices
| Page | What it contains | Open |
|---|---|---|
| Company jobs | Active postings from Uscareers Lumanity Icims Com. | Open |
| Company breakdowns | Role, location, ATS, and work model facets for this company. | Open |
| ATS provider jobs | Active postings observed through iCIMS. | Open |
| Provider filtered search | The same provider as a filtered job collection. | Open |
| Department jobs | Active postings in Clinical and Regulatory. | Open |
| Work model jobs | Active Remote postings. | Open |
| Lifecycle events | Open, update, close, and reopen events for this posting. | Open |
| Original posting | Canonical source or apply URL captured from the ATS. | Open |
Linked records
| Company | Uscareers Lumanity Icims Com |
| Source | bba0af74-984e-42aa-968c-d2bb748b5bc8 |
| ATS provider | iCIMS |
Description
Overview/About Lumanity
Lumanity is dedicated to improving health outcomes by accelerating and optimizing access to life-changing medicines. As a global strategic partner that brings together strategy, evidence, engagement, and technology, we were designed to engineer breakthrough value to tackle our clients’ toughest challenges by revolutionizing how value is generated, demonstrated, and communicated.
Responsibilities / Position overview
The Vice President, Regulatory Strategy is a senior enterprise leader who combines deep regulatory technical expertise with proven consulting and biopharma experience to drive practice growth and deliver transformational regulatory strategies for VP and C-suite client executives. This role partners with the SVP & Practice Lead to shape the future direction of Lumanity's Clinical & Regulatory practice while maintaining direct accountability for revenue growth, client relationships, and team development across global markets.
The VP serves as a senior regulatory authority, translating regulatory landscape evolution into practice opportunities, building unique competitive capabilities, and positioning the firm as the go-to regulatory strategy authority for complex, high-stakes pharmaceutical development programs.
Essential Duties/Responsibilities:
Strategic Leadership & Client Partnership
Acts as trusted strategic partner to pharmaceutical and biotech C-suite executives and other functional heads, influencing enterprise-wide regulatory strategies that extend across multiple development programs and corporate initiatives
Provides authoritative regulatory guidance on complex, multi-indication development programs, including novel modalities (cell/gene therapy, biologics, advanced therapeutics)
Partners with other Lumanity practices to deliver integrated solutions addressing interconnected regulatory, clinical, and quality challenges
Practice Strategy & Innovation
Partners with SVP & Practice Lead to translate regulatory landscape changes (AI/digital submissions, global harmonization, policy evolution) into practice growth opportunities and competitive differentiation
Develops regulatory points of view that influence industry standards, shapes regulatory policy dialogue, and positions Lumanity as the authoritative voice in regulatory strategy consulting
Evolves consulting methodologies and develops new service offerings to address emerging regulatory challenges and client needs
Commercial Accountability & Growth
Proactively supports the Clinical & Regulatory P&L, in collaboration with the SVP and Practice Lead, achieving annual revenue targets while maintaining target profitability margins
Dives personal and team BD performance, leading pursuit strategies for complex, high-value regulatory engagements while mentoring BD capability across the practice
Delivery Excellence & Team Leadership
Sets and reinforces delivery quality standards across regulatory team, ensuring consistency in regulatory strategy outputs while balancing profitability with client value
Shapes regulatory talent strategy through succession planning, mentorship of senior regulatory leaders, and development of next-generation regulatory capabilities
Champions collaboration and knowledge sharing across markets, accelerating reuse of regulatory frameworks and best practices
Market Presence & External Influence
Represents Lumanity at senior industry forums and regulatory conferences building external credibility and market presence
Monitors regulatory competitive landscape and translates insights into practice positioning and service evolution
Qualifications
Minimum 20+ years progressive regulatory experience with demonstrated success in both consulting environments and in-house biopharma regulatory leadership roles
Direct experience leading regulatory strategies for development programs throughout all stages and across different therapeutic areas and product types
Demonstrated success managing regulatory practices or teams
Proven ability to serve as trusted advisor to pharmaceutical/biotech VP-level and C-suite executives
Deep expertise across pre-IND through post-market regulatory activities, including designations, accelerated approval pathways, and complex regulatory strategies
Extensive experience leading Pre-IND meetings, Type C meetings, EOP2 discussions, and other critical regulatory interactions
International regulatory experience across major markets (EMA, Health Canada, PMDA) with understanding of global regulatory harmonization
Deep regulatory expertise in 2+ major therapeutic areas (oncology, CNS, rare disease, immunology, etc.)
Experience across multiple product types including small molecules, biologics, cell/gene therapies, and combination products
PhD, MPH, or MS in life sciences, regulatory affairs, or related field
MBA, RAC certification, or equivalent business/regulatory qualifications
Proven track record achieving annual revenue targets with demonstrated budget management experience
Success in opening new markets or service lines within regulatory consulting
Published regulatory thought leadership, speaking engagements, and recognition as regulatory industry authority
Benefits
We offer our employees a comprehensive benefits package that focuses on what matters to you – health and well-being, personal finances, professional development, and a healthy work/life balance:
Competitive salary plus bonus scheme
Medical, dental, and vision insurance options
401(k) plan with employer match
Flexible PTO
Flexible spending accounts for health and dependent care
Health savings account option with employer contribution
Employee Assistance Program
Paid short-term and long-term disability coverage and much more
-----------------------------------------------------------------------------
#LI-remote
Full job record
| Job ID | 9639de2cb4ac2cdc4ae65765d4c331a169c63bf8 |
| Org ID | 5516b56f-0740-490b-a171-f573fb1d285c |
| Source ID | bba0af74-984e-42aa-968c-d2bb748b5bc8 |
| Board ID | bba0af74-984e-42aa-968c-d2bb748b5bc8 |
| Provider | icims |
| Provider Job Key | 2103 |
| Title | Vice President, Regulatory Strategy |
| Normalized Title | — |
| Status | active |
| Active | yes |
| Location Text | Remote, UNAVAILABLE, US |
| Department | Clinical and Regulatory |
| Team | — |
| Employment Type | OTHER |
| Workplace Type | remote |
| Remote Policy | remote |
| Country | United States |
| Region | UNAVAILABLE |
| City | — |
| Salary Raw | Overview/About Lumanity Lumanity is dedicated to improving health outcomes by accelerating and optimizing access to life-changing medicines. As a global strategic partner that brings together strategy, evidence, engagement, and technology, we were designed to engineer breakthrough value to tackle our clients’ toughest challenges by revolutionizing how value is generated, demonstrated, and communicated. Responsibilities / Position overview The Vice President, Regulatory Strategy is a senior enterprise leader who combines deep regulatory technical expertise with proven consulting and biopharma experience to drive practice growth and deliver transformational regulatory strategies for VP and C-suite client executives. This role partners with the SVP & Practice Lead to shape the future direction of Lumanity's Clinical & Regulatory practice while maintaining direct accountability for revenue growth, client relationships, and team development across global markets. The VP serves as a senior regulatory authority, translating regulatory landscape evolution into practice opportunities, building unique competitive capabilities, and positioning the firm as the go-to regulatory strategy authority for complex, high-stakes pharmaceutical development programs. Essential Duties/Responsibilities: Strategic Leadership & Client Partnership Acts as trusted strategic partner to pharmaceutical and biotech C-suite executives and other functional heads, influencing enterprise-wide regulatory strategies that extend across multiple development programs and corporate initiatives Provides authoritative regulatory guidance on complex, multi-indication development programs, including novel modalities (cell/gene therapy, biologics, advanced therapeutics) Partners with other Lumanity practices to deliver integrated solutions addressing interconnected regulatory, clinical, and quality challenges Practice Strategy & Innovation Partners with SVP & Practice Lead to translate regulatory landscape changes (AI/digital submissions, global harmonization, policy evolution) into practice growth opportunities and competitive differentiation Develops regulatory points of view that influence industry standards, shapes regulatory policy dialogue, and positions Lumanity as the authoritative voice in regulatory strategy consulting Evolves consulting methodologies and develops new service offerings to address emerging regulatory challenges and client needs Commercial Accountability & Growth Proactively supports the Clinical & Regulatory P&L, in collaboration with the SVP and Practice Lead, achieving annual revenue targets while maintaining target profitability margins Dives personal and team BD performance, leading pursuit strategies for complex, high-value regulatory engagements while mentoring BD capability across the practice Delivery Excellence & Team Leadership Sets and reinforces delivery quality standards across regulatory team, ensuring consistency in regulatory strategy outputs while balancing profitability with client value Shapes regulatory talent strategy through succession planning, mentorship of senior regulatory leaders, and development of next-generation regulatory capabilities Champions collaboration and knowledge sharing across markets, accelerating reuse of regulatory frameworks and best practices Market Presence & External Influence Represents Lumanity at senior industry forums and regulatory conferences building external credibility and market presence Monitors regulatory competitive landscape and translates insights into practice positioning and service evolution Qualifications Minimum 20+ years progressive regulatory experience with demonstrated success in both consulting environments and in-house biopharma regulatory leadership roles Direct experience leading regulatory strategies for development programs throughout all stages and across different therapeutic areas and product types Demonstrated success managing regulatory practices or teams Proven ability to serve as trusted advisor to pharmaceutical/biotech VP-level and C-suite executives Deep expertise across pre-IND through post-market regulatory activities, including designations, accelerated approval pathways, and complex regulatory strategies Extensive experience leading Pre-IND meetings, Type C meetings, EOP2 discussions, and other critical regulatory interactions International regulatory experience across major markets (EMA, Health Canada, PMDA) with understanding of global regulatory harmonization Deep regulatory expertise in 2+ major therapeutic areas (oncology, CNS, rare disease, immunology, etc.) Experience across multiple product types including small molecules, biologics, cell/gene therapies, and combination products PhD, MPH, or MS in life sciences, regulatory affairs, or related field MBA, RAC certification, or equivalent business/regulatory qualifications Proven track record achieving annual revenue targets with demonstrated budget management experience Success in opening new markets or service lines within regulatory consulting Published regulatory thought leadership, speaking engagements, and recognition as regulatory industry authority Benefits We offer our employees a comprehensive benefits package that focuses on what matters to you – health and well-being, personal finances, professional development, and a healthy work/life balance: Competitive salary plus bonus scheme Medical, dental, and vision insurance options 401(k) plan with employer match Flexible PTO Flexible spending accounts for health and dependent care Health savings account option with employer contribution Employee Assistance Program Paid short-term and long-term disability coverage and much more ----------------------------------------------------------------------------- #LI-remote |
| Salary Min | — |
| Salary Max | — |
| Salary Currency | — |
| Salary Period | — |
| Source URL | https://uscareers-lumanity.icims.com/jobs/2103/vice-president%2c-regulatory-strategy/job |
| Apply URL | https://uscareers-lumanity.icims.com/jobs/2103/vice-president%2c-regulatory-strategy/job |
| First Seen At | 2026-05-31 18:46:41Z |
| Last Seen At | 2026-06-06 08:34:51Z |
| Last Checked At | 2026-06-06 08:34:51Z |
| Last Changed At | 2026-06-01 14:05:15Z |
| Inactive At | — |
| Source Posted At | 2026-05-08 04:00:00Z |
| Source Updated At | 2026-05-08 07:57:45Z |
| Raw Payload Uri | s3://job-postings-prod-raw-590183727216/raw/provider=icims/board=uscareers-lumanity.icims.com/date=2026-06-06/2026-06-06T08-34-50-682Z-29ad99aa01b21c7641ec204f207335bf11f1e188b980bd7cfed2ca0573bbcbee.json |
Event Fields
{
"content_hash": "ba43c4a76aa21704623cb9e4268656d73229eb92ff4a8db93b00a2764772f984",
"source_hash": "ea08594c0ce2b2362d11d0404b8842563f7e32fe82d9bfb69472b60884558157",
"last_changed_at": "2026-06-01T14:05:15.648Z",
"active_status": "active"
}Parsed Structured
{
"language": "en",
"location": {
"raw": "Remote, UNAVAILABLE, US",
"city": null,
"region": "UNAVAILABLE",
"country": "United States",
"is_remote": true,
"confidence": 0.8
},
"salary_max": null,
"salary_min": null,
"inferred_at": "2026-06-06T08:34:51.419Z",
"launch_scope": {
"reason": "english_us_canada",
"included": true,
"language": "en",
"location": {
"raw": "Remote, UNAVAILABLE, US",
"city": null,
"region": "UNAVAILABLE",
"country": "United States",
"is_remote": true,
"confidence": 0.8
},
"countries": [
"United States"
]
},
"remote_policy": "remote",
"salary_period": null,
"workplace_type": "remote",
"salary_currency": null
}Extensions
{}Native Structured
{
"json_ld": {
"url": "https://uscareers-lumanity.icims.com/jobs/2103/vice-president%2c-regulatory-strategy/job",
"@type": "JobPosting",
"title": "Vice President, Regulatory Strategy",
"@context": "http://schema.org",
"datePosted": "2026-05-08T04:00:00.000Z",
"description": "<h2>Overview/About Lumanity</h2>\n<p>Lumanity is dedicated to improving health outcomes by accelerating and optimizing access to life-changing medicines. As a global strategic partner that brings together strategy, evidence, engagement, and technology, we were designed to engineer breakthrough value to tackle our clients’ toughest challenges by revolutionizing how value is generated, demonstrated, and communicated.</p>\n<h2>Responsibilities / Position overview</h2>\n<p>The Vice President, Regulatory Strategy is a senior enterprise leader who combines deep regulatory technical expertise with proven consulting and biopharma experience to drive practice growth and deliver transformational regulatory strategies for VP and C-suite client executives. This role partners with the SVP & Practice Lead to shape the future direction of Lumanity's Clinical & Regulatory practice while maintaining direct accountability for revenue growth, client relationships, and team development across global markets.</p>\n<p> </p>\n<p>The VP serves as a senior regulatory authority, translating regulatory landscape evolution into practice opportunities, building unique competitive capabilities, and positioning the firm as the go-to regulatory strategy authority for complex, high-stakes pharmaceutical development programs.</p>\n<p> </p>\n<p><strong><u>Essential Duties/Responsibilities:</u></strong></p>\n<p><strong> </strong></p>\n<p><strong>Strategic Leadership & Client Partnership</strong></p>\n<ul>\n <li>Acts as trusted strategic partner to pharmaceutical and biotech C-suite executives and other functional heads, influencing enterprise-wide regulatory strategies that extend across multiple development programs and corporate initiatives</li>\n <li>Provides authoritative regulatory guidance on complex, multi-indication development programs, including novel modalities (cell/gene therapy, biologics, advanced therapeutics)</li>\n <li>Partners with other Lumanity practices to deliver integrated solutions addressing interconnected regulatory, clinical, and quality challenges</li>\n</ul>\n<p><strong> </strong></p>\n<p><strong>Practice Strategy & Innovation</strong></p>\n<ul>\n <li>Partners with SVP & Practice Lead to translate regulatory landscape changes (AI/digital submissions, global harmonization, policy evolution) into practice growth opportunities and competitive differentiation</li>\n <li>Develops regulatory points of view that influence industry standards, shapes regulatory policy dialogue, and positions Lumanity as the authoritative voice in regulatory strategy consulting</li>\n <li>Evolves consulting methodologies and develops new service offerings to address emerging regulatory challenges and client needs</li>\n</ul>\n<p><strong> </strong></p>\n<p><strong>Commercial Accountability & Growth</strong></p>\n<ul>\n <li>Proactively supports the Clinical & Regulatory P&L, in collaboration with the SVP and Practice Lead, achieving annual revenue targets while maintaining target profitability margins</li>\n <li>Dives personal and team BD performance, leading pursuit strategies for complex, high-value regulatory engagements while mentoring BD capability across the practice</li>\n</ul>\n<p><strong>Delivery Excellence & Team Leadership</strong></p>\n<ul>\n <li>Sets and reinforces delivery quality standards across regulatory team, ensuring consistency in regulatory strategy outputs while balancing profitability with client value</li>\n <li>Shapes regulatory talent strategy through succession planning, mentorship of senior regulatory leaders, and development of next-generation regulatory capabilities</li>\n <li>Champions collaboration and knowledge sharing across markets, accelerating reuse of regulatory frameworks and best practices</li>\n</ul>\n<p> </p>\n<p><strong>Market Presence & External Influence</strong></p>\n<ul>\n <li>Represents Lumanity at senior industry forums and regulatory conferences building external credibility and market presence</li>\n <li>Monitors regulatory competitive landscape and translates insights into practice positioning and service evolution</li>\n</ul>\n<h2>Qualifications</h2>\n<ul>\n <li>Minimum 20+ years progressive regulatory experience with demonstrated success in both consulting environments and in-house biopharma regulatory leadership roles</li>\n <li>Direct experience leading regulatory strategies for development programs throughout all stages and across different therapeutic areas and product types</li>\n <li>Demonstrated success managing regulatory practices or teams</li>\n <li>Proven ability to serve as trusted advisor to pharmaceutical/biotech VP-level and C-suite executives</li>\n <li>Deep expertise across pre-IND through post-market regulatory activities, including designations, accelerated approval pathways, and complex regulatory strategies</li>\n <li>Extensive experience leading Pre-IND meetings, Type C meetings, EOP2 discussions, and other critical regulatory interactions</li>\n <li>International regulatory experience across major markets (EMA, Health Canada, PMDA) with understanding of global regulatory harmonization</li>\n <li>Deep regulatory expertise in 2+ major therapeutic areas (oncology, CNS, rare disease, immunology, etc.)</li>\n <li>Experience across multiple product types including small molecules, biologics, cell/gene therapies, and combination products</li>\n <li>PhD, MPH, or MS in life sciences, regulatory affairs, or related field</li>\n <li>MBA, RAC certification, or equivalent business/regulatory qualifications</li>\n <li>Proven track record achieving annual revenue targets with demonstrated budget management experience</li>\n <li>Success in opening new markets or service lines within regulatory consulting</li>\n <li>Published regulatory thought leadership, speaking engagements, and recognition as regulatory industry authority</li>\n</ul>\n<h2>Benefits</h2>\n<p>We offer our employees a comprehensive benefits package that focuses on what matters to you – health and well-being, personal finances, professional development, and a healthy work/life balance:</p>\n<ul>\n <li>Competitive salary plus bonus scheme</li>\n <li>Medical, dental, and vision insurance options</li>\n <li>401(k) plan with employer match</li>\n <li>Flexible PTO</li>\n <li>Flexible spending accounts for health and dependent care</li>\n <li>Health savings account option with employer contribution</li>\n <li>Employee Assistance Program</li>\n <li>Paid short-term and long-term disability coverage and much more</li>\n</ul>\n<h2>-----------------------------------------------------------------------------</h2>\n<p>#LI-remote</p>",
"directApply": true,
"jobLocation": [
{
"@type": "Place",
"address": {
"@type": "PostalAddress",
"postalCode": "UNAVAILABLE",
"addressRegion": "UNAVAILABLE",
"streetAddress": "UNAVAILABLE",
"addressCountry": "US",
"addressLocality": "Remote",
"postOfficeBoxNumber": "UNAVAILABLE"
}
}
],
"validThrough": "2027-05-08T04:00:00.000Z",
"employmentType": "OTHER",
"hiringOrganization": {
"name": "Lumanity",
"@type": "Organization",
"sameAs": "UNAVAILABLE"
},
"occupationalCategory": "Clinical and Regulatory"
},
"detail_meta": {
"url": "https://uscareers-lumanity.icims.com/jobs/2103/vice-president%2c-regulatory-strategy/job?in_iframe=1",
"http_status": 200,
"content_type": "text/html;charset=UTF-8",
"response_bytes": 38641,
"compact_response_bytes": 7685,
"original_response_bytes": 38641
},
"sitemap_job": {
"id": "2103",
"url": "https://uscareers-lumanity.icims.com/jobs/2103/vice-president%2c-regulatory-strategy/job",
"slug": "vice-president%2c-regulatory-strategy",
"lastmod": "2026-05-08T03:57:45-04:00"
},
"detail_errors": []
}Get this page with API
Rendered from the bluedoor Job Postings API. Reproduce it:
GET https://api.bluedoor.sh/job-postings/v1/jobs/9639de2cb4ac2cdc4ae65765d4c331a169c63bf8?include=descriptionJSONGET https://api.bluedoor.sh/job-postings/v1/orgs/5516b56f-0740-490b-a171-f573fb1d285cJSONGET https://api.bluedoor.sh/job-postings/v1/sources/bba0af74-984e-42aa-968c-d2bb748b5bc8JSONGET https://api.bluedoor.sh/job-postings/v1/jobs/9639de2cb4ac2cdc4ae65765d4c331a169c63bf8/eventsJSON