Medical Director Jobs in New Jersey
Medical Director jobs in New Jersey are among the most active in the northeast, concentrated in health systems, pharmaceuticals, managed care, and academic medicine, with openings at every level from newly appointed physician leaders through senior executive roles. The heaviest hiring is in Newark, Princeton, and Morristown, where employers like RWJBarnabas Health, Hackensack Meridian Health, and Johnson and Johnson maintain large and lasting operations. The most in-demand specialties are utilization management, population health, and clinical operations leadership. Find a role that fits below and apply directly.
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About Summit:
Summit Therapeutics Inc. is a biopharmaceutical oncology company with a mission focused on improving quality of life, increasing potential duration of life, and resolving serious unmet medical needs. At Summit, we believe in building a team of world class professionals who are passionate about this mission, and it is our people who drive this mission to reality. Summit's core values include integrity, passion for excellence, purposeful urgency, collaboration, and our commitment to people. Our employees are truly the heart and soul of our culture, and they are invaluable in shaping our journey toward excellence.
Summit's team is inspired to touch and help change lives through Summit's clinical studies in the field of oncology. Summit has multiple global Phase 3 clinical studies, including:
Non-small Cell Lung Cancer (NSCLC)
HARMONi: Phase 3 clinical study which was intended to evaluate ivonescimab combined with chemotherapy compared to placebo plus chemotherapy in patients with EGFR-mutated, locally advanced or metastatic non-squamous NSCLC who were previously treated with a 3rd generation EGFR TKI.
HARMONi-3: Phase 3 clinical study which is intended to evaluate ivonescimab combined with chemotherapy compared to pembrolizumab combined with chemotherapy in patients with first-line metastatic NSCLC.
HARMONi-7: Phase 3 clinical study which is intended to evaluate ivonescimab monotherapy compared to pembrolizumab monotherapy in patients with first-line metastatic NSCLC.
Colorectal Cancer (CRC)
HARMONi-GI3: Phase 3 clinical study intended to evaluate ivonescimab in combination with chemotherapy compared with bevacizumab plus chemotherapy.
Ivonescimab is an investigational therapy not presently approved by any regulatory authority other than China's National Medical Products Administration (NMPA). Summit is headquartered in Miami, Florida, and has additional offices in California, New Jersey, the UK, and Ireland.
Overview of Role
The Director, Medical Affairs Operations will lead the global Medical Affairs Operations function and provide strategic oversight for the execution of operational activities that support Medical Affairs strategy across regions. This role serves as a key business partner to Medical Affairs leadership and collaborates closely with Compliance, Legal, Finance, Clinical Development, and external vendors to ensure consistent, compliant, and efficient execution of congress sponsorships, advisory boards, scientific engagement programs, healthcare professional interactions, vendor management, contracting, budgeting, systems, and operational excellence initiatives. The Director will establish scalable processes, drive global alignment, manage vendor relationships, build operational capabilities, and oversee a global team supporting Global Medical Affairs operations, while supporting launch readiness, organizational growth, and the successful execution of strategic initiatives across the Medical Affairs organization.
Responsibilities
- Global Medical Affairs Operations Leadership: Lead operational planning and execution of Medical Affairs initiatives across regions, therapeutic areas, and functions. Establish scalable frameworks, policies, processes, and best practices that improve efficiency, quality, compliance, and organizational readiness.
- Team Leadership and Development: Lead, coach, and develop a high-performing global Medical Affairs Operations team, including congress sponsorship, US operations, and Europe-based operations roles. Establish goals, performance objectives, development plans, and operating rhythms that support team effectiveness and future growth.
- Cross-Functional Partnership and Governance: Partner with regional Medical Affairs leaders, Compliance, Legal, Regulatory Affairs, Finance, Procurement, Clinical Development, IT, and external vendors. Ensure consistent execution of operational processes worldwide and act as an escalation point for operational challenges and cross-functional issue resolution.
- Vendor and Financial Management: Oversee Medical Affairs vendor strategy, selection, contracting, performance management, SOWs, purchase orders, budgets, forecasting, and invoice reconciliation. Partner with Finance and Procurement to optimize resource utilization and ensure external engagements follow FMV requirements, company policies, and industry standards.
- Congress, Advisory Board, and Scientific Engagement Operations: Provide oversight for national, regional, and international congress sponsorships, exhibits, medical booths, scientific exchange activities, advisory boards, investigator meetings, and individual customer engagements. Establish standardized planning processes, operational metrics, vendor oversight, and resource plans to support consistent execution across regions.
- Compliance and Operational Risk Management: Ensure Medical Affairs operations adhere to healthcare compliance requirements, Sunshine Act reporting obligations, FMV standards, company policies, and applicable industry regulations. Maintain audit-ready documentation, monitor emerging requirements, and identify operational risks with appropriate mitigation plans.
- Systems, Metrics, and Analytics: Lead development and implementation of dashboards, reports, KPIs, and operational metrics to measure program effectiveness, congress investments, vendor performance, and operational activities. Partner with IT and Digital teams to implement systems and use analytics to identify process improvements and resource allocation opportunities.
- Strategic Planning and Launch Readiness: Support annual planning, budget planning, long-range Medical Affairs operational strategy, pipeline expansion, and new product launch readiness. Develop resource and infrastructure plans that enable growth across regions, functions, and therapeutic areas.
Experience, Education and Specialized Knowledge and Skills:
- Bachelor's degree in Life Sciences, Healthcare, Business Administration, or related field required.
- Advanced degree (MS, MBA, MPH, PharmD, or equivalent) preferred.
- 10+ years of experience in Medical Affairs Operations, Clinical Operations, Commercial Operations, or related pharmaceutical/biotech functions.
- Minimum 5 years of people management experience.
- Oncology experience strongly preferred.
- Experience supporting both US and international Medical Affairs organizations preferred.
- Demonstrated experience supporting pre-launch and launch-stage organizations.
- Proven experience managing complex vendor relationships, operational budgets, and cross-functional initiatives.
- Strong leadership and team development capabilities.
- Excellent project and portfolio management skills.
- Deep understanding of healthcare compliance requirements, FMV processes, Sunshine Act reporting, and contracting practices.
- Strong financial and budget management expertise.
- Ability to operate effectively in a fast-paced, matrixed biotech environment.
- Experience implementing operational systems, dashboards, and process improvement initiatives.
- Strong analytical and problem-solving skills with a focus on operational excellence.
Actual compensation packages are based on several factors that are unique to each candidate, including but not limited to skill set, depth of experience, certifications, and specific work location. This may be different in other locations due to differences in the cost of labor. The total compensation package for this position may also include bonus, stock, benefits and/or other applicable variable compensation.
Summit does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact Summit's Talent Acquisition team at recruiting@smmttx.com to obtain prior written authorization before referring any candidates to Summit.
Summit Therapeutics Inc. is an Equal Opportunity Employer and takes pride in creating and maintaining diverse environment. We do not discriminate in recruitment, hiring, training or promotion or any other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, marital or veteran status, disability, or any other legally protected status.
About Summit:
Summit Therapeutics Inc. is a biopharmaceutical oncology company with a mission focused on improving quality of life, increasing potential duration of life, and resolving serious unmet medical needs. At Summit, we believe in building a team of world class professionals who are passionate about this mission, and it is our people who drive this mission to reality. Summit's core values include integrity, passion for excellence, purposeful urgency, collaboration, and our commitment to people. Our employees are truly the heart and soul of our culture, and they are invaluable in shaping our journey toward excellence.
Summit's team is inspired to touch and help change lives through Summit's clinical studies in the field of oncology. Summit has multiple global Phase 3 clinical studies, including:
Non-small Cell Lung Cancer (NSCLC)
HARMONi: Phase 3 clinical study which was intended to evaluate ivonescimab combined with chemotherapy compared to placebo plus chemotherapy in patients with EGFR-mutated, locally advanced or metastatic non-squamous NSCLC who were previously treated with a 3rd generation EGFR TKI.
HARMONi-3: Phase 3 clinical study which is intended to evaluate ivonescimab combined with chemotherapy compared to pembrolizumab combined with chemotherapy in patients with first-line metastatic NSCLC.
HARMONi-7: Phase 3 clinical study which is intended to evaluate ivonescimab monotherapy compared to pembrolizumab monotherapy in patients with first-line metastatic NSCLC.
Colorectal Cancer (CRC)
HARMONi-GI3: Phase 3 clinical study intended to evaluate ivonescimab in combination with chemotherapy compared with bevacizumab plus chemotherapy.
Ivonescimab is an investigational therapy not presently approved by any regulatory authority other than China's National Medical Products Administration (NMPA). Summit is headquartered in Miami, Florida, and has additional offices in California, New Jersey, the UK, and Ireland.
Overview of Role
The Director, Medical Affairs Operations will lead the global Medical Affairs Operations function and provide strategic oversight for the execution of operational activities that support Medical Affairs strategy across regions. This role serves as a key business partner to Medical Affairs leadership and collaborates closely with Compliance, Legal, Finance, Clinical Development, and external vendors to ensure consistent, compliant, and efficient execution of congress sponsorships, advisory boards, scientific engagement programs, healthcare professional interactions, vendor management, contracting, budgeting, systems, and operational excellence initiatives. The Director will establish scalable processes, drive global alignment, manage vendor relationships, build operational capabilities, and oversee a global team supporting Global Medical Affairs operations, while supporting launch readiness, organizational growth, and the successful execution of strategic initiatives across the Medical Affairs organization.
Responsibilities
- Global Medical Affairs Operations Leadership: Lead operational planning and execution of Medical Affairs initiatives across regions, therapeutic areas, and functions. Establish scalable frameworks, policies, processes, and best practices that improve efficiency, quality, compliance, and organizational readiness.
- Team Leadership and Development: Lead, coach, and develop a high-performing global Medical Affairs Operations team, including congress sponsorship, US operations, and Europe-based operations roles. Establish goals, performance objectives, development plans, and operating rhythms that support team effectiveness and future growth.
- Cross-Functional Partnership and Governance: Partner with regional Medical Affairs leaders, Compliance, Legal, Regulatory Affairs, Finance, Procurement, Clinical Development, IT, and external vendors. Ensure consistent execution of operational processes worldwide and act as an escalation point for operational challenges and cross-functional issue resolution.
- Vendor and Financial Management: Oversee Medical Affairs vendor strategy, selection, contracting, performance management, SOWs, purchase orders, budgets, forecasting, and invoice reconciliation. Partner with Finance and Procurement to optimize resource utilization and ensure external engagements follow FMV requirements, company policies, and industry standards.
- Congress, Advisory Board, and Scientific Engagement Operations: Provide oversight for national, regional, and international congress sponsorships, exhibits, medical booths, scientific exchange activities, advisory boards, investigator meetings, and individual customer engagements. Establish standardized planning processes, operational metrics, vendor oversight, and resource plans to support consistent execution across regions.
- Compliance and Operational Risk Management: Ensure Medical Affairs operations adhere to healthcare compliance requirements, Sunshine Act reporting obligations, FMV standards, company policies, and applicable industry regulations. Maintain audit-ready documentation, monitor emerging requirements, and identify operational risks with appropriate mitigation plans.
- Systems, Metrics, and Analytics: Lead development and implementation of dashboards, reports, KPIs, and operational metrics to measure program effectiveness, congress investments, vendor performance, and operational activities. Partner with IT and Digital teams to implement systems and use analytics to identify process improvements and resource allocation opportunities.
- Strategic Planning and Launch Readiness: Support annual planning, budget planning, long-range Medical Affairs operational strategy, pipeline expansion, and new product launch readiness. Develop resource and infrastructure plans that enable growth across regions, functions, and therapeutic areas.
Experience, Education and Specialized Knowledge and Skills:
- Bachelor's degree in Life Sciences, Healthcare, Business Administration, or related field required.
- Advanced degree (MS, MBA, MPH, PharmD, or equivalent) preferred.
- 10+ years of experience in Medical Affairs Operations, Clinical Operations, Commercial Operations, or related pharmaceutical/biotech functions.
- Minimum 5 years of people management experience.
- Oncology experience strongly preferred.
- Experience supporting both US and international Medical Affairs organizations preferred.
- Demonstrated experience supporting pre-launch and launch-stage organizations.
- Proven experience managing complex vendor relationships, operational budgets, and cross-functional initiatives.
- Strong leadership and team development capabilities.
- Excellent project and portfolio management skills.
- Deep understanding of healthcare compliance requirements, FMV processes, Sunshine Act reporting, and contracting practices.
- Strong financial and budget management expertise.
- Ability to operate effectively in a fast-paced, matrixed biotech environment.
- Experience implementing operational systems, dashboards, and process improvement initiatives.
- Strong analytical and problem-solving skills with a focus on operational excellence.
Actual compensation packages are based on several factors that are unique to each candidate, including but not limited to skill set, depth of experience, certifications, and specific work location. This may be different in other locations due to differences in the cost of labor. The total compensation package for this position may also include bonus, stock, benefits and/or other applicable variable compensation.
Summit does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact Summit's Talent Acquisition team at recruiting@smmttx.com to obtain prior written authorization before referring any candidates to Summit.
Summit Therapeutics Inc. is an Equal Opportunity Employer and takes pride in creating and maintaining diverse environment. We do not discriminate in recruitment, hiring, training or promotion or any other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, marital or veteran status, disability, or any other legally protected status.
See All 120+ Medical Director Jobs in New Jersey
Find roles in New Jersey that match your experience and apply in just a few clicks.
Find Medical Director JobsMedical Director Jobs by City in New Jersey
Where New Jersey roles are concentrated, by current openings.
Medical Director Job Market in New Jersey
A snapshot from current New Jersey openings, updated as new roles post.
Who's Hiring
Top Industries Hiring
- Biotechnology & Pharmaceuticals
- Healthcare & Medical Services
- Education
- Energy
- Manufacturing
What New Jersey Employers Look For
The qualifications that appear most often in medical director jobs across New Jersey.
- Active and unrestricted medical license issued by the New Jersey State Board of Medical Examiners
- MD or DO degree from an accredited medical school with completed residency training
- Board certification in a specialty relevant to the department or clinical program
- Minimum of five years of clinical practice experience in a relevant specialty area
- Demonstrated leadership experience including supervision of clinical staff or program oversight
- Familiarity with utilization management, quality improvement, and regulatory compliance standards
Medical Director Jobs in New Jersey: Frequently Asked Questions
How do you become a medical director in New Jersey?
You must hold an active, unrestricted medical license issued by the New Jersey State Board of Medical Examiners, which requires completing medical school, residency, and passing the USMLE or COMLEX. Beyond licensure, most New Jersey employers expect board certification in your specialty and several years of clinical practice before moving into a director role. Building experience in quality improvement, utilization review, or department leadership within a New Jersey health system is the most direct path to a first medical director position.
Which companies hire medical directors in New Jersey?
Employers hiring medical directors in New Jersey right now include Insmed Incorporated, AbbVie, and Concentra, based on current listings on Migrate Mate as of October 2026. New Jersey's concentration of large academic health systems, pharmaceutical headquarters, and managed care organizations means medical director openings appear across both clinical and corporate settings throughout the state.
Which New Jersey cities have the most medical director jobs?
Bridgewater, Princeton, and New Jersey have the most medical director openings in New Jersey. Newark anchors the market through its major academic medical centers and health system headquarters, while Princeton draws corporate medical director roles from the pharmaceutical and managed care companies clustered in central New Jersey, and Morristown reflects the dense suburban hospital activity across Morris County.
Are there remote medical director jobs in New Jersey?
Yes, but they are less common than in purely analytical fields because many medical director roles require on-site clinical oversight, committee participation, or direct staff supervision. About 69% of medical director openings tied to New Jersey are remote or hybrid as of October 2026, reflecting that some flexibility exists. Utilization management and managed care medical director positions are the most likely to offer remote or hybrid arrangements among New Jersey employers.
How can I get hired as a medical director in New Jersey with little or no experience?
The most realistic entry path is moving into a physician leadership role within a New Jersey health system before applying to a formal medical director title. RWJBarnabas Health and Hackensack Meridian Health both offer physician leadership development programs and frequently post associate medical director or department chief roles that serve as stepping stones. Lateral moves from roles like medical officer, department chair, or quality and patient safety physician are the most common transitions. Completing a graduate degree in health administration or obtaining board certification in medical management strengthens a candidacy significantly.
Where can I find and apply to medical director jobs in New Jersey?
You can find and apply to medical director jobs in New Jersey on Migrate Mate, which lists current openings across the state. Find roles that fit your specialty, experience level, and preferred location, and apply directly to each one.
See All 120+ Medical Director Jobs in New Jersey
Find roles in New Jersey that match your experience and apply in just a few clicks.
Find Medical Director Jobs