Market Director Visa Sponsorship Jobs in New Jersey
Market director visa sponsorship jobs in New Jersey are concentrated along the Route 1 corridor and in cities like Princeton, Newark, and Hoboken, where pharmaceutical giants like Johnson & Johnson and Novo Nordisk, financial firms, and consumer brands headquartered in the state regularly sponsor senior marketing leadership roles.
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About AbbVie
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on LinkedIn, Facebook, Instagram, X and YouTube.
Job Description
The Senior Director, Pipeline Market Access Strategy (PMAX) is a newly created role responsible for leading and inspiring the end-to-end global market access strategy for pipeline assets within their assigned Business Unit. This position will require strong enterprise leadership to navigate the organization through multiple external environment pressures on global pharmaceutical pricing and reimbursement.
This role bridges early asset development and future commercialization readiness, ensuring that pricing and access considerations are embedded from the earliest stages of the drug development lifecycle and through Phase 3 design and identification of evidence needs. The Senior Director serves as the definitive voice of pipeline market access, shaping clinical trial design, evidence generation, and target product profiles through a global access and reimbursement lens. Importantly this position will need to define distinct US and international strategies to optimize global launch success.
The Senior Director will lead a team of experts across both US Pipeline Strategy and International Pipeline Strategy and will have an opportunity to define the objectives and vision for the team appropriately. This role will provide leadership across both domestic and global dimensions of pipeline access, partnering deeply with inline US and International access teams as well as R&D, Regulatory, HEOR, Global Commercial Development, Business Development, and Government Affairs to deliver integrated access strategies that position AbbVie's pipeline for long-term commercial and patient-access success.
Key Responsibilities
Pipeline Access Strategy & Portfolio Leadership
- Owns the end-to-end pipeline Integrated access strategy for all pre-launch and development-stage assets within the assigned Business Unit, ensuring strategies are comprehensive in addressing evidence needs, policy considerations, pricing potential, and commercial considerations. IASs integrate global needs and dynamics through regulatory submission.
- Serves as the primary voice of pipeline market access strategies at Business Unit governance forums, including LMG, TASC, CSM, ASTs, and other senior leadership reviews — communicating access risk, opportunity, and strategic direction with clarity and conviction.
- Serves as the voice of access into pipeline Business Development opportunities.
- Leads prioritization exercises across the pipeline portfolio to ensure resources and strategic attention are allocated to assets with the greatest near- and long-term access complexity and business impact.
- Creates and optimizes launch strategies inclusive of considerations for IRA, MFN, and other market forces (US Channel dynamics) to position the asset for sequencing strategies across indications as well as geographies incorporating the pressures.
- Defines and delivers the Access Roadmap—a cross-functionally developed strategy that articulates the access approach for each pipeline asset by development phase, anticipated launch timing, and global evidence deliverables.
Early Development Integration
- Partners with R&D and Regulatory teams to embed access-relevant endpoints, comparators, and trial design elements into clinical development programs from Phase I/II onward — ensuring studies are powered to meet payer and HTA evidence standards at launch and partners with the affiliates.
- Defines and champions Target Product Profiles (TPPs) from a market access perspective, translating payer value requirements into actionable clinical and evidence generation guidance for asset teams.
- Generates and maintains global payer and HTA evidence requirements across major markets (US, EU5, Japan, and emerging markets), ensuring development programs proactively address the evidence gaps that govern access and reimbursement decisions.
US & International Strategy Alignment
- Provides strategic leadership and direction to the US Pipeline Strategy Lead and International Pipeline Strategy Lead, ensuring both domestic and global perspectives are fully integrated into a cohesive, Business Unit-level pipeline access strategy.
- Aligns US payer strategy, formulary positioning, and value communication frameworks with international HTA, pricing, and reimbursement approaches — creating a globally consistent access narrative that can flex to local market requirements.
- Anticipates cross-market reference pricing dynamics, parallel trade risks, and HTA precedent effects, incorporating these considerations into early pipeline access strategy to protect long-term portfolio value across geographies.
- Partners closely with US and International Pipeline Strategy Leads to develop and execute a structured pipeline-to-launch transition framework, ensuring that market access strategies, payer evidence packages, and reimbursement submissions are fully prepared ahead of regulatory approval.
- Collaborates with US and international commercial, medical, and market access teams to ensure seamless knowledge transfer and strategic handoff at the point of regulatory approval — including payer communication plans, launch sequencing strategies, and country-level access readiness assessments.
- Leads cross-functional launch readiness reviews in partnership with US and International teams to identify and resolve access gaps (evidence, pricing approvals, formulary positioning) prior to approval, ensuring no delays to patient access at launch.
- Ensures that affiliate and in-country market access teams are equipped with globally aligned value messages, health economic tools, and reimbursement dossiers well in advance of launch — bridging the transition from pipeline to commercial ownership.
Cross-Functional Leadership & Partnership
- Provides strategic direction and partnership to cross-functional groups including HEOR, R&D, Regulatory, Global Commercial Development, Global Marketing, Government Affairs, and Business Development — ensuring market access perspectives are fully integrated into all pipeline asset decisions.
- Leads the development of Integrated Evidence Plans (IEPs) in close collaboration with HEOR, ensuring real-world evidence, health economic modeling, and outcomes research strategies are aligned with anticipated payer and HTA requirements at launch.
- Partners with Government Affairs to anticipate and shape the evolving policy and reimbursement landscape, embedding policy risk and opportunity assessments into pipeline access strategies.
- Collaborates with Global Commercial Development and Global Marketing to ensure pipeline access strategies are aligned with brand positioning, indication sequencing, and long-range commercial forecasts.
Business Development & Asset Evaluation
- Works closely with Business Development to inform the market access potential of in-licensing, partnership, and acquisition opportunities — providing rigorous payer landscape assessments, reimbursement probability analyses, and access risk evaluations to support BD decision-making.
- Establishes and communicates access-based licensing priorities, ensuring that pipeline expansion decisions account for payer value evidence requirements, competitive access dynamics, and global pricing sustainability.
- Serves as the access subject matter expert in due diligence processes, assessing the payer readiness and evidence maturity of externally sourced pipeline assets being evaluated for AbbVie's portfolio.
Governance, Stakeholder Engagement & People Leadership
- Represents pipeline market access priorities at senior leadership governance forums, portfolio review committees, and cross-Business Unit strategy sessions — serving as the definitive voice on access considerations that should inform pipeline investment and development decisions.
- Builds, develops, and retains a high-performing pipeline access team, providing mentorship, career development, and performance management for direct and indirect reports across US and international functions.
- Fosters a culture of innovation, rigor, and affiliate-centricity within the pipeline access team — ensuring that affiliate launch needs, in-country market dynamics, and local payer requirements are actively incorporated into global strategy development.
Qualifications
Education
- An advanced degree (MBA, MPH, PhD, PharmD, or equivalent) in business, health economics, public policy, life sciences, or a related field is required.
- Formal training or demonstrated expertise in health technology assessment (HTA), health economics, outcomes research, or pharmaceutical development is strongly preferred.
- Bachelor's degree in a scientific, business, or public health discipline is required as a minimum baseline.
Experience
- A minimum of 12–15 years of progressive, senior-level experience in market access, pricing, reimbursement, HEOR, or a closely related pharmaceutical/biopharmaceutical function — with a substantial portion of that experience focused on pipeline and pre-launch strategy.
- Demonstrated expertise in global market access, including a deep working knowledge of HTA processes, payer evidence requirements, pricing and reimbursement frameworks, and access decision-making dynamics across major international markets (US, EU5, Japan, and additional key markets).
- Proven experience shaping clinical development strategy from a market access and outcomes evidence perspective — including direct experience contributing to clinical trial design, endpoint selection, and Integrated Evidence Plan development in collaboration with R&D teams.
- Strong track record of leading and developing high-performing teams in a matrixed, multinational environment, with demonstrated ability to manage direct reports and influence cross-functional partners without direct authority.
- Experience supporting Business Development activities including asset due diligence, licensing evaluations, and access-based valuation assessments is highly preferred.
- Comfortable operating at the senior leadership level, with demonstrated ability to communicate complex access strategy to executive audiences and influence enterprise-level pipeline investment decisions.
- Experience across multiple therapeutic areas (e.g., Oncology, Immunology, Neuroscience) is an asset, though deep expertise in at least one is required.
Key Competencies
- Strategic Vision & Access Leadership
- Global HTA & Payer Expertise
- Clinical Development Partnership
- Evidence Generation Strategy
- Cross-Functional Influence
- Pipeline Portfolio Prioritization
- Business Development Acumen
- US/International Strategy Alignment
- People Leadership & Talent Development
- Executive Communication & Governance
Additional Information
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:
- The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future.
- We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.
- This job is eligible to participate in our long-term incentive programs.
Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and may be modified at the Company’s sole and absolute discretion, consistent with applicable law.
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.
US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html
US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
https://www.abbvie.com/join-us/reasonable-accommodations.html
Company Description
About AbbVie
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on LinkedIn, Facebook, Instagram, X and YouTube.
Job Description
The Senior Director, Pipeline Market Access Strategy (PMAX) is a newly created role responsible for leading and inspiring the end-to-end global market access strategy for pipeline assets within their assigned Business Unit. This position will require strong enterprise leadership to navigate the organization through multiple external environment pressures on global pharmaceutical pricing and reimbursement.
This role bridges early asset development and future commercialization readiness, ensuring that pricing and access considerations are embedded from the earliest stages of the drug development lifecycle and through Phase 3 design and identification of evidence needs. The Senior Director serves as the definitive voice of pipeline market access, shaping clinical trial design, evidence generation, and target product profiles through a global access and reimbursement lens. Importantly this position will need to define distinct US and international strategies to optimize global launch success.
The Senior Director will lead a team of experts across both US Pipeline Strategy and International Pipeline Strategy and will have an opportunity to define the objectives and vision for the team appropriately. This role will provide leadership across both domestic and global dimensions of pipeline access, partnering deeply with inline US and International access teams as well as R&D, Regulatory, HEOR, Global Commercial Development, Business Development, and Government Affairs to deliver integrated access strategies that position AbbVie's pipeline for long-term commercial and patient-access success.
Key Responsibilities
Pipeline Access Strategy & Portfolio Leadership
- Owns the end-to-end pipeline Integrated access strategy for all pre-launch and development-stage assets within the assigned Business Unit, ensuring strategies are comprehensive in addressing evidence needs, policy considerations, pricing potential, and commercial considerations. IASs integrate global needs and dynamics through regulatory submission.
- Serves as the primary voice of pipeline market access strategies at Business Unit governance forums, including LMG, TASC, CSM, ASTs, and other senior leadership reviews — communicating access risk, opportunity, and strategic direction with clarity and conviction.
- Serves as the voice of access into pipeline Business Development opportunities.
- Leads prioritization exercises across the pipeline portfolio to ensure resources and strategic attention are allocated to assets with the greatest near- and long-term access complexity and business impact.
- Creates and optimizes launch strategies inclusive of considerations for IRA, MFN, and other market forces (US Channel dynamics) to position the asset for sequencing strategies across indications as well as geographies incorporating the pressures.
- Defines and delivers the Access Roadmap—a cross-functionally developed strategy that articulates the access approach for each pipeline asset by development phase, anticipated launch timing, and global evidence deliverables.
Early Development Integration
- Partners with R&D and Regulatory teams to embed access-relevant endpoints, comparators, and trial design elements into clinical development programs from Phase I/II onward — ensuring studies are powered to meet payer and HTA evidence standards at launch and partners with the affiliates.
- Defines and champions Target Product Profiles (TPPs) from a market access perspective, translating payer value requirements into actionable clinical and evidence generation guidance for asset teams.
- Generates and maintains global payer and HTA evidence requirements across major markets (US, EU5, Japan, and emerging markets), ensuring development programs proactively address the evidence gaps that govern access and reimbursement decisions.
US & International Strategy Alignment
- Provides strategic leadership and direction to the US Pipeline Strategy Lead and International Pipeline Strategy Lead, ensuring both domestic and global perspectives are fully integrated into a cohesive, Business Unit-level pipeline access strategy.
- Aligns US payer strategy, formulary positioning, and value communication frameworks with international HTA, pricing, and reimbursement approaches — creating a globally consistent access narrative that can flex to local market requirements.
- Anticipates cross-market reference pricing dynamics, parallel trade risks, and HTA precedent effects, incorporating these considerations into early pipeline access strategy to protect long-term portfolio value across geographies.
- Partners closely with US and International Pipeline Strategy Leads to develop and execute a structured pipeline-to-launch transition framework, ensuring that market access strategies, payer evidence packages, and reimbursement submissions are fully prepared ahead of regulatory approval.
- Collaborates with US and international commercial, medical, and market access teams to ensure seamless knowledge transfer and strategic handoff at the point of regulatory approval — including payer communication plans, launch sequencing strategies, and country-level access readiness assessments.
- Leads cross-functional launch readiness reviews in partnership with US and International teams to identify and resolve access gaps (evidence, pricing approvals, formulary positioning) prior to approval, ensuring no delays to patient access at launch.
- Ensures that affiliate and in-country market access teams are equipped with globally aligned value messages, health economic tools, and reimbursement dossiers well in advance of launch — bridging the transition from pipeline to commercial ownership.
Cross-Functional Leadership & Partnership
- Provides strategic direction and partnership to cross-functional groups including HEOR, R&D, Regulatory, Global Commercial Development, Global Marketing, Government Affairs, and Business Development — ensuring market access perspectives are fully integrated into all pipeline asset decisions.
- Leads the development of Integrated Evidence Plans (IEPs) in close collaboration with HEOR, ensuring real-world evidence, health economic modeling, and outcomes research strategies are aligned with anticipated payer and HTA requirements at launch.
- Partners with Government Affairs to anticipate and shape the evolving policy and reimbursement landscape, embedding policy risk and opportunity assessments into pipeline access strategies.
- Collaborates with Global Commercial Development and Global Marketing to ensure pipeline access strategies are aligned with brand positioning, indication sequencing, and long-range commercial forecasts.
Business Development & Asset Evaluation
- Works closely with Business Development to inform the market access potential of in-licensing, partnership, and acquisition opportunities — providing rigorous payer landscape assessments, reimbursement probability analyses, and access risk evaluations to support BD decision-making.
- Establishes and communicates access-based licensing priorities, ensuring that pipeline expansion decisions account for payer value evidence requirements, competitive access dynamics, and global pricing sustainability.
- Serves as the access subject matter expert in due diligence processes, assessing the payer readiness and evidence maturity of externally sourced pipeline assets being evaluated for AbbVie's portfolio.
Governance, Stakeholder Engagement & People Leadership
- Represents pipeline market access priorities at senior leadership governance forums, portfolio review committees, and cross-Business Unit strategy sessions — serving as the definitive voice on access considerations that should inform pipeline investment and development decisions.
- Builds, develops, and retains a high-performing pipeline access team, providing mentorship, career development, and performance management for direct and indirect reports across US and international functions.
- Fosters a culture of innovation, rigor, and affiliate-centricity within the pipeline access team — ensuring that affiliate launch needs, in-country market dynamics, and local payer requirements are actively incorporated into global strategy development.
Qualifications
Education
- An advanced degree (MBA, MPH, PhD, PharmD, or equivalent) in business, health economics, public policy, life sciences, or a related field is required.
- Formal training or demonstrated expertise in health technology assessment (HTA), health economics, outcomes research, or pharmaceutical development is strongly preferred.
- Bachelor's degree in a scientific, business, or public health discipline is required as a minimum baseline.
Experience
- A minimum of 12–15 years of progressive, senior-level experience in market access, pricing, reimbursement, HEOR, or a closely related pharmaceutical/biopharmaceutical function — with a substantial portion of that experience focused on pipeline and pre-launch strategy.
- Demonstrated expertise in global market access, including a deep working knowledge of HTA processes, payer evidence requirements, pricing and reimbursement frameworks, and access decision-making dynamics across major international markets (US, EU5, Japan, and additional key markets).
- Proven experience shaping clinical development strategy from a market access and outcomes evidence perspective — including direct experience contributing to clinical trial design, endpoint selection, and Integrated Evidence Plan development in collaboration with R&D teams.
- Strong track record of leading and developing high-performing teams in a matrixed, multinational environment, with demonstrated ability to manage direct reports and influence cross-functional partners without direct authority.
- Experience supporting Business Development activities including asset due diligence, licensing evaluations, and access-based valuation assessments is highly preferred.
- Comfortable operating at the senior leadership level, with demonstrated ability to communicate complex access strategy to executive audiences and influence enterprise-level pipeline investment decisions.
- Experience across multiple therapeutic areas (e.g., Oncology, Immunology, Neuroscience) is an asset, though deep expertise in at least one is required.
Key Competencies
- Strategic Vision & Access Leadership
- Global HTA & Payer Expertise
- Clinical Development Partnership
- Evidence Generation Strategy
- Cross-Functional Influence
- Pipeline Portfolio Prioritization
- Business Development Acumen
- US/International Strategy Alignment
- People Leadership & Talent Development
- Executive Communication & Governance
Additional Information
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:
- The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future.
- We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.
- This job is eligible to participate in our long-term incentive programs.
Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and may be modified at the Company’s sole and absolute discretion, consistent with applicable law.
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.
US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html
US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
https://www.abbvie.com/join-us/reasonable-accommodations.html
Market Director Job Roles in New Jersey
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Search Market Director Jobs in New JerseyMarket Director Jobs in New Jersey: Frequently Asked Questions
Which companies sponsor visas for market directors in New Jersey?
New Jersey's pharmaceutical and life sciences sector produces the most consistent sponsorship activity for market director roles. Johnson & Johnson, Novo Nordisk, Synchronoss Technologies, and Conduent have all filed H-1B visa Labor Condition Applications for senior marketing positions. Consumer goods companies like Church & Dwight and Bed Bath & Beyond's legacy successors, as well as financial services firms in Newark and Jersey City, also appear in DOL disclosure data for marketing leadership roles.
Which visa types realistically fit market director roles in New Jersey?
Market director roles qualify as specialty occupations when they require a bachelor's degree in marketing, business, or a related field, making H-1B the primary path. Australian nationals can pursue the E-3 visa under the same specialty occupation standard. Chilean nationals may use the H-1B1 visa and Singapore nationals the H-1B1 (Singapore), both of which have uncapped allocations. A green card via EB-2 or EB-3 is also an option for candidates with employer support and sufficient experience.
Which cities in New Jersey have the most market director sponsorship jobs?
Princeton and its surrounding Mercer County corridor lead for pharmaceutical and biotech marketing leadership, anchored by major corporate campuses. Newark draws financial services and insurance sector roles, while Hoboken and Jersey City benefit from proximity to New York City, attracting marketing positions from media, technology, and consumer brands with tri-state area operations. Parsippany and Bridgewater also host regional headquarters with active marketing leadership teams.
How to find market director visa sponsorship jobs in New Jersey?
Migrate Mate lists market director roles in New Jersey with verified employer sponsorship history, so you can focus on companies that have actively filed for marketing leadership positions rather than applying broadly. Because market director titles vary across industries, searching by both exact title and related marketing leadership terms on Migrate Mate helps surface the full range of sponsoring employers active in the state's pharmaceutical, financial, and consumer goods sectors.
Are there state-specific factors that affect market director sponsorship in New Jersey?
New Jersey's dense concentration of pharmaceutical and life sciences headquarters means market director roles here often require sector-specific expertise, particularly in healthcare marketing and product commercialization. The state's proximity to major academic institutions including Rutgers University also creates a pipeline of candidates familiar with regulated industry marketing. Employers in regulated sectors tend to document specialty occupation requirements carefully, which can strengthen the H-1B petition for senior marketing roles.
What is the prevailing wage for sponsored market director jobs in New Jersey?
U.S. employers sponsoring a visa must pay at least the prevailing wage, which is what workers in the same role, area, and experience level typically earn. The Department of Labor sets this rate to make sure companies aren't hiring foreign workers simply because they'd accept lower pay than a U.S. worker. It varies by job title, location, and experience. You can look up current prevailing wage rates for any occupation and location using the OFLC Wage Search page.