480 Results for

Director Of Regulatory Affairs Jobs in New York

Jobs

New York

Direct IND lifecycle management experience: you have owned INDs from filing through amendment cycles, authored DSURs, prepared IB updates, and built FDA meeting packages as the primary author. That means authoring DSURs, preparing IB updates and IND amendments, building FDA meeting packages, managing ClinicalTrials.gov listings, and overseeing eCTD publishing.

30+ days ago

$231,000–$285,000 / year

Overview of Role: The Executive Director of Regulatory Affairs - Global Regulatory Leader, is responsible for developing and implementing global strategies to secure IND/CTA approvals for various studies as well as providing regulatory leadership for planning and execution of subsequent global marketing applications (BLA/MAA) for product(s) in the oncology therapeutic area. 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.

28 days ago

New York

Remote

Conducts precedent searches, analyzes relevant analogs or competitor labeling, labeling guidance and trends; and develops labeling language for inclusion to assigned product labels (TLP, CCDS, USPI, when applicable EU SmPC,) to ensure consistency with the overall product strategy, product claims and information in the CCDS. Leads Labeling cross-functional working group (LWG) and interacts with cross-functional senior leadership to resolve complex issues, including leading and contributing to cross-functional initiatives by providing expertise in labeling best practices.

30+ days ago

Remote

$176,400–$207,500 / year

Create and follow procedures for regulatory execution and implementation of regulatory strategies while actively supporting program leads via the Clinical Study Teams (CSTs) to deliver on business objectives for assigned products/programs (e.g. Powered by proprietary multimodal data, purpose-built AI models, and bilingual teams fluent in both science and AI, the Recursion OS is designed to translate complex science into medicines that matter faster, better, and at scale for patients who are waiting.

30+ days ago

$146,700–$196,700 / year

Provides strategic and operational regulatory direction on assigned projects including, but not limited to general regulatory strategies, regulatory requirements for clinical studies and marketing approval, risk assessments, critical issue management and advice on health authority interactions. Excellent verbal and written skills; able to analyze, define, and effectively convey difficult and complex issues in a way that accurately and persuasively communicates the issues to internal and external stakeholders.

30+ days ago

Remote

$225,000–$250,000 / year

30+ days ago

$240,000–$275,000 / year

This role oversees end-to-end planning and delivery of global clinical submissions, leads the creation and release of core regulatory dossiers, drives country-level customization strategies, and ensures high-quality responses to regulatory RFIs to support timely trial startup and advancement. Nektar currently anticipates the base salary for the Senior Specialist, Clinical Regulatory Affairs to range from $240,000 to $275,000 for candidates in the Bay Area and will depend, in part, on successful candidate''s location and qualifications for the role, including education and experience.

19 days ago

Remote

$176,400–$228,250 / year

Powered by proprietary multimodal data, purpose-built AI models, and bilingual teams fluent in both science and AI, the Recursion OS is designed to translate complex science into medicines that matter - faster, better, and at scale - for patients who are waiting. Recursion is advancing a portfolio of differentiated investigational medicines across its wholly owned and partnered pipeline in oncology, rare disease, neuroscience, immunology, and other therapeutic areas with significant unmet need.

30+ days ago

$253,000–$312,500 / year

This role will develop and implement regulatory strategies leading to successful registration and life-cycle management of unique and technologically complex products serving patients with cancer and other unmet medical needs. • Provide regulatory advice and guidance in the context of available and expected scientific data, regulatory guidance, and precedent to project teams to support decision making and program advancement.

30+ days ago

Remote

$157,200–$256,600 / year

Perform final review and approval of the compliance activities of the portfolios to confirm regulatory impact and associated submission requirements for clinical and commercial regulatory filings in accordance with country-specific regulatory guidance documents; • Mentor colleagues in difficult compliance assessment discussions with SMEs or Senior Management; find opportunities for improvement of processes for compliance tasks. • Critically review and provide meaningful and strategic input on regulatory filing documents (e.g., INDs, IMPDs, meeting packages, scientific advice, BLAs, MAAs, BPDRs, annual reports, DSUR, amendments, supplements) to facilitate and expedite the development, licensure, and marketing of drugs and/or biologics.

30+ days ago

Remote - Any State US, NY

Remote

$190,000–$200,000 / year

We are looking for an experienced hands-on Regulatory Affairs professional to contribute to the development strategy and lead in the planning, preparation, submission and maintenance of regulatory submissions for Nuvation products. Our full-time regular positions also include an annual performance-based bonus and long-term incentive units (equity) provided as part of our compensation package, in addition to a full range of medical, financial, and/or other benefits, depending on the level and position offered.

1 day ago

$205,000–$341,600 / year

The Director will develop and maintain regulatory strategy at the study, indication, and program level, lead interactions with global health authorities, and serve as a key cross-functional partner and subject matter expert. Working with cross-functional project teams to resolve complex regulatory issues, utilizing deep expertise in global regulations and guidances to strategically plan and communicate requirements.

8 days ago

$204,500–$274,500 / year

Provide strategic and operational leadership for the development and execution of global biologics Regulatory CMC strategies for the responsible regions, including oversight of authoring, review, and lifecycle management of CMC sections of CTDs (Modules 2 and 3) for INDs, BLAs, MAAs, and post approval submissions. This role provides strategic and operational leadership for U.S.-based biologics Regulatory CMC activities and serves as a key partner to the China-based counterpart and global cross-functional stakeholders in the development and execution of global CMC regulatory strategies across the product lifecycle.

30+ days ago

$142,000–$192,000 / year

Manage, prepare, and/or author CMC document packages for global regulatory submissions in support of development and lifecycle programs, including primary authorship and/or leadership of Module 3 (Quality) sections for INDs, CTAs, IMPDs, BLAs, MAAs, supplements, and variations. Fosters Teamwork Provides and Solicits Honest and Actionable Feedback Self-Awareness Acts Inclusively Demonstrates Initiative Entrepreneurial Mindset Continuous Learning Embraces Change Results-Oriented Analytical Thinking/Data Analysis Financial Excellence Communicates with Clarity.

30+ days ago

$135,600–$237,400 / year

Job Summary: The Regulatory Affairs Director is responsible for leading activities of the Regulatory Affairs Department, including contracts, compliance, surveys, audits, investigations, reporting, plan development and renewal, credentialing, Fraud, Waste & Abuse Special Investigations, provider network and relations, regulatory updates and compliance matters. CareSource takes into consideration a combination of a candidate's education, training, and experience as well as the position's scope and complexity, the discretion and latitude required for the role, and other external and internal data when establishing a salary level.

22 days ago

$190,000–$240,000 / year

The Director- Compliance Coordination and Regulatory Affairs is a senior role within the Compliance Team responsible for the following functions:Regulatory Engagement & Examination ManagementServe as Compliance primary point of contact for U.S. regulatory agencies during examinations, inquiries, and ongoing supervisory activities;Coordinate and manage end-to-end regulatory examinations, including preparation, document production, regulatory meetings, and remediation efforts;Develop and maintain examination response protocols and methodology;Track and manage regulatory requests to ensure timely, accurate, and complete responses;Review and challenge regulatory deliverables;Support regulatory inquiries and examinations in the Americas and across business lines as needed;Internal Audit CoordinationPartner with Internal Audit to coordinate compliance-related audit reviews;Manage audit response processes, including deliverables validation and review;Strategic Project LeadershipLead and contribute to high-priority compliance projects and department-wide initiatives;Collaborate with cross-functional teams to implement compliance program enhancements;Drive process improvements and automation opportunities within the compliance function;Stakeholder ManagementBuild and maintain productive relationships with regulatory agencies;Partner with other divisions (business lines/support functions) on compliance matters;Provide regular updates to senior leadership on regulatory developments and examination status. This team has a number of different functions, but its primary functions are the management of interactions with US Regulators, management of compliance projects, tracking and reporting of issues, quality assurance, regulatory watch and support to regulatory changes, compliance communication, and regulatory coordination.

30+ days ago

$228,000–$233,000 / year

The Director, Global Regulatory Affairs will provide leadership on ex-US regulatory activities for Protara's product portfolio, and responsibility will focus on clinical study applications and provide regulatory leadership on the project teams in this area. The Company is evaluating TARA-002 in an ongoing Phase 2 trial in NMIBC patients with carcinoma in situ (CIS) who are unresponsive or naïve to treatment with Bacillus Calmette-Guérin (BCG), as well as a Phase 2 trial in pediatric patients with LMs.

30+ days ago

New York, NY

$95,450–$143,175 / year

The Director of Regulatory & Administrative Affairs for the Mount Sinai Institute for Transformative Clinical Trials provides strategic leadership and operational oversight for regulatory, safety, and administrative activities supporting a portfolio of sponsor-led, investigator-initiated, federally funded, and industry-sponsored clinical research studies. Mount Sinai advances health for all people, everywhere, by taking on the most complex health care challenges of our time - discovering and applying new scientific learning and knowledge; developing safer, more effective treatments; educating the next generation of medical leaders and innovators; and supporting local communities by delivering high-quality care to all who need it.

1 day ago

$180,000–$280,000 / year

Consistently named a best place to work, Click fosters an inclusive, diverse workforce of innovators, clinicians, scientists, researchers, designers, technologists, engineers and more, united in a common mission to provide patients everywhere access to safe and effective prescription digital therapeutics. Click Therapeutics may at its business discretion decide to or refrain from obtaining, maintaining and/or extending the temporary visa status and/or sponsoring a colleague for permanent residency and /or employment eligibility, considering factors such as availability of qualified U.S. workers and the colleague's long-term prospects for securing lawful permanent residence, among other reasons.

30+ days ago

$128,600–$210,000 / year

Help lead and assist in all interactions with the FDA Office of Prescription drug Promotion (OPDP) for assigned company products, responsible for helping to maintain working relationship and effective communication with FDA OPDP reviewers with respect to advertising and promotion matters, including request for advisory submissions. Provide timely regulatory advice and guidance, with guidance from Regulatory Affairs, Advertising & Promotion Director, to Commercial teams and Medical Affairs with respect to conference exhibit activities, disease awareness and speaker programs.

30+ days ago

New York, NY

$175,000–$225,000 / year

Reporting to the Chief Medical Officer, this leader will elevate Cellectis’ scientific presence, support pipeline advancement, and ensure medical excellence in evidence generation, scientific communications, and external engagement. Cellectis is seeking a highly experienced Senior Director, Medical Affairs to help shape and operationalize the company’s medical affairs strategy across its clinical‑stage portfolio.

30+ days ago

New York

Lead/assist with Corrective and Preventative Action (CAPA) investigations, plan development and implementation of corrective actions, author CAPA reports, and ensure completion and accuracy of all associated Quality records. Administration of Document Control function, including document ID issuance, revision control, coordination of review and approval, communication of implementation tasks, and maintenance of all records.

30+ days ago

Albany, New York

The position will design and implement state-level advocacy strategies aligned with enterprise priorities and will manage engagement with key stakeholders and execution of public affairs initiatives as directed and designed in collaboration with Corporate Affairs leadership. Serves as the company’s primary representative at the assigned state capitols before executive leadership, including Medicaid directors, transportation program leaders, and personal care services (PCS) administrators.

30+ days ago

New York, NY

Remote

$152,000–$230,000 / year

Proven ability to lead cross-program or cross-organizational strategy in complex, matrixed settings, building trust and influence without direct authority and working through ambiguity Exceptional writing skills, with demonstrated ability to translate complex policy or research content into clear, compelling narratives. By the end of the first 12 months, a successful Executive Director, EaR Strategy and Alignment Partner will have: Established themselves as a trusted, credible embedded partner to GPER, L&A, HMA, and other policy-adjacent teams, with a consistent presence at leadership tables and strong executive-level relationships.

1 day ago

$175,000–$225,000 / year

Reporting to the Chief Medical Officer, this leader will elevate Cellectis' scientific presence, support pipeline advancement, and ensure medical excellence in evidence generation, scientific communications, and external engagement. Cellectis is seeking a highly experienced Senior Director, Medical Affairs to help shape and operationalize the company's medical affairs strategy across its clinical-stage portfolio.

30+ days ago

$159,900–$215,900 / year

The position will design and implement state-level advocacy strategies aligned with enterprise priorities and will manage engagement with key stakeholders and execution of public affairs initiatives as directed and designed in collaboration with Corporate Affairs leadership. Serves as the companys primary representative at the assigned state capitols before executive leadership, including Medicaid directors, transportation program leaders, and personal care services (PCS) administrators.

30+ days ago

New York City, NY

Remote

$79,488–$104,328 / year

Manage the end-to-end administrative lifecycle of each dispute by maintaining real-time updates on project management boards, gathering and redacting member documentation, and uploading supporting evidence to the appropriate portal stages within set regulatory deadlines. Work Location: This is a remote position, open to candidates who reside in: Arizona, Florida, Georgia, Illinois, Iowa, Kansas, Michigan, Missouri, Nebraska, New Jersey, New York, North Carolina, Ohio, Pennsylvania, South Carolina, Tennessee, Texas and Virginia.

26 days ago

Remote

$79,488–$104,328 / year

30+ days ago

Tonawanda, NY

Product development and launch: Support product development and commercial launch activities, including process and formulation development, protocol design and execution, and engineering runs; participate in the development of project timelines and tracking of deliverables; and identify and help resolve technical, resource, or scheduling constraints with internal teams and external vendors. Position Summary The Pharmacist - Pharmacy Services/Regulatory Affairs supports the Director of Pharmacy Services & Regulatory Affairs in ensuring that Pine Pharmaceuticals' products are developed, tested, manufactured, marketed, and distributed in compliance with applicable federal and state regulatory requirements.

3 days ago

$333,300–$450,900 / year

This role might be for you if: • Must have an MD or MD equivalent with a preference for specialized fellowship training in Gastroenterology or Hepatology • 5 years of related industry experience in global or US medical affairs • Solid background and experience in drug development and life-cycle management • Experience with working in an alliance setting strongly preferred • Ability to lead technical and business discussions internally and externally and explain scientific/medical concepts to all levels • Ability to cultivate and maintain relationships with leading medical/scientific experts in the relevant fields • Ability to establish trust through the consistent demonstration of scientific expertise and satisfactory follow-through on requests from key opinion leaders • Strong leadership and management skills • Attention to detail in analyses, deliverables, and communications • Strong presentation and communication skills; must be able to provide succinct, strategic, and actionable insights to senior management • A proactive self-starter who can lead work and manage others independently, with the ability to see the next step and take actions without prompting • Ability to juggle multiple projects • Thorough understanding of the healthcare environment including all external stakeholders. A typical day in this role might look like: • Provides visionary leadership in the development, execution, and continuous refinement of medical strategy and tactics for assigned assets, ensuring alignment with corporate and global objectives.

30+ days ago

Washington, New York

$110,000–$125,000 / year

We lead integrated campaigns across media, stakeholder engagement, advocacy, research and paid media, coordinating seamlessly across internal teams and external partners to drive outcomes for clients across healthcare, nonprofits, technology, land use, education, infrastructure and other sectors. You will collaborate across public affairs, PR, digital, content, paid media and community engagement teams to build integrated programs that connect online engagement with real-world impact, including public sentiment, stakeholder alignment and policy outcomes.

23 days ago

Anywhere, NY

Remote

$153,541–$230,312 / year

The current base salary range for this position is expected to be between $153,541 and $230,312 annualized; final salary will be determined based on various factors including, but not limited to, years of relevant experience, job knowledge, skills and proficiency, degree/education, and internal comparators. Our team’s proven track record of executional excellence, combined with our depth of expertise and dedication, enables us to develop innovative medicines that reflect the priorities of rare disease communities.

15 days ago

New York, NY

$85,000–$130,000 / year

The Manager/Director of Board Governance & Executive Affairs serves as a trusted partner to executive leadership and the Boards of Directors across The Fedcap Group, providing governance leadership, executive operations support, and stakeholder engagement across the organization. This individual will serve as a key liaison between executive leadership, board members, Executive Directors, and external stakeholders while ensuring seamless coordination of board activities, governance initiatives, executive priorities, and strategic engagement efforts.

Today

Remote

$330,000–$364,000 / year

Mineralys Therapeutics is a clinical-stage biopharmaceutical company focused on developing medicines to target hypertension and related comorbidities such as chronic kidney disease (CKD), obstructive sleep apnea (OSA) and other diseases driven by dysregulated aldosterone. The Senior Director, Medical Affairs will serve as a strategic and scientific leader responsible for shaping and executing the global medical affairs strategy in support of the company's pipeline and future commercial products.

30+ days ago

$176,100–$287,300 / year

As an Associate Director, Field Medical Affairs, you will serve as the primary scientific presence in your territory, engaging in meaningful exchange of clinical data and medical information with KOLs, HCPs, clinical research investigators, pharmacists, and other decision makers. Responding to requests for information related to study indications, disease states, and the therapeutic area, and discussing scientific and clinical data with appropriate audiences in a compliant manner.

30 days ago

New York, NY

$180,000–$280,000 / year

26 days ago

$296,600–$376,600 / year

In addition to leading the strategy and executional elements of phase IV (post-marketing) and investigator-initiated studies programs, the role includes broad collaboration with colleagues from clinical development and commercial, in particular for launch preparation and execution, and to ensure that cross-functional plans and activities benefit from the insight of an experienced clinician. In alignment with the VP Hematology Lead, GMA, works closely with and acts as an internal medical, clinical, and practice subject matter expert for internal teams seeking medical input into drug- or non-drug-related projects and strategic planning, including.

30+ days ago

$325,000–$425,000 / year

Recognizing that this development bottleneck may ultimately limit the number of new medicines that can reach patients, Formation Bio, founded in 2016 as TrialSpark Inc., has built technology platforms, processes, and capabilities to accelerate all aspects of drug development and clinical trials. Formation Bio partners, acquires, or in-licenses drugs from pharma companies, research organizations, and biotechs to develop programs past clinical proof of concept and beyond, ultimately helping to bring new medicines to patients.

30+ days ago

$220,000–$230,000 / year

Oversee agreements and collaborations with affiliates, partners, and other institutions Support the Office of Assessment Develop and manage assigned budgets Collaborates with Human Resources in faculty counseling and management of faculty grievance and appeals processes in alignment with Long Island University, Lewyt College of Veterinary Medicine mission areas. Vice Dean of Academic Affairs, Lewyt College of Veterinary MedicineVice Dean of Academic Affairs, Lewyt College of Veterinary Medicine No. 4526 Long Island University Brookville, New York Dean - Veterinary Medicine Posted Jan 23, 2026 $220,000 - $230,000.

30+ days ago

$175,000–$240,000 / year

This role provides strategic scientific leadership to advance ACMs long-term vision, translating organizational strategy into high-impact scientific execution across global teams of scientists, PhDs, and R&D professionals. Serving as the internal and external scientific ambassador for ACM, the role partners closely with senior leadership, clients, and industry stakeholders to identify gaps, develop innovative scientific solutions, and strengthen service offerings.

30+ days ago

$175,000–$240,000 / year

Serving as the internal and external scientific ambassador for ACM, the role partners closely with senior leadership, clients, and industry stakeholders to identify gaps, develop innovative scientific solutions, and strengthen service offerings. This role provides strategic scientific leadership to advance ACM's long-term vision, translating organizational strategy into high-impact scientific execution across global teams of scientists, PhDs, and R&D professionals.

30+ days ago

$222,300–$255,000 / year

This includes, but is not limited to, providing scientific and methodological expertise to support medical strategy, publications, and external engagements; serving as the primary point of contact between biostatistics and the Medical Affairs team; collaborating with the team in development of publication strategy plans; maintaining and executing Supplemental Statistical Analysis Plans (SAPs); and assisting as needed with real-world evidence-generating requests. They interact with both internal and external cross-functional study teams to support the scientific communication effort, and partner with unblinded biometrics study team members to deliver needed statistical output in a timely fashion.

30+ days ago

$175,000–$210,000 / year

Partner with Marketing Internal Medicine Category Lead and other Veterinary Professional Services colleagues to contribute to, or lead if delegated, key tactical customer activities and meetings based on brand strategy plans (e.g., advisory board meetings, speakers'' bureaus, professional association relationship management, KOL development and engagement, segmented customer education/training). Create and/or guide agency or Key Opinion Leader (KOL) generated technical content for products across the aligned portfolio; serve as a subject matter expert in the medical review of brand-aligned content within the Ad and Promotional Review process.

13 days ago

$159,000–$219,000 / year

We are seeking a dynamic and experienced Associate Director of Global Field Medical Training & Excellence to enhance the performance and capabilities of our Field Medical teams worldwide with a focus in the U.S. This critical role integrates therapy area expertise, Field Medical business acumen, and advanced training methodologies to deliver impactful learning initiatives that align with Biogen's medical goals for field-facing employees. Regular employees are eligible to receive both short term and long-term incentives, including cash bonus and equity incentive opportunities, designed to reward recent achievements and recognize your future potential based on individual, business unit and company performance.

4 days ago

$144,300–$194,300 / year

This role will focus on engineering and operationalizing AI systems-including Retrieval-Augmented Generation (RAG), agentic AI frameworks, and LLM-powered services-enabling teams across Commercial, Medical, and other functions to build and deploy AI solutions in a secure, scalable, and reusable manner. As a key technology leader, you will define and drive the AI platform strategy, developer experience, and enablement frameworks, ensuring seamless integration with BeOne's modular technology stack (data platforms, CRM, marketing systems, and analytics environments).

30+ days ago

$150,000–$190,000 / year

Work with the relevant internal departments in all regulatory and government issues relating to the digital exploitation of WCM's compositions Provide reports and present on complex digital licensing matters to senior executives Contribute to global digital strategy for Warner Chappell, with emphasis on how the strategy will impact on or be impacted by changes at a regulatory or legislative level About you: A minimum of four years of relevant transactional legal experience At least two years of direct work experience negotiating digital licensing agreements in-house at a music company, media company, or technology company licensing music or other content, or at a law firm J.D. and active license to practice in relevant jurisdiction Understanding of and experience with content licensing, digital media, and intellectual property law and the legal implications of AI Strong negotiation skills and experience (in particular, the ability to lead and manage negotiations with a multiplicity of parts), as well as strong analytical and organizational skills Refined and well-practiced drafting skills (in particular, the ability to develop and draft legal provisions that address creative solutions in area with evolving legal guidance) Attention to detail and the ability to manage a high-volume workload efficiently and effectively Strong familiarity with new technology developments, including AI, and related legal issues Effective and confident communication skills Experience working across multiple time zones We'd love it if you also had: A passion for the intersection of music, business, law, and technology Experience negotiating license agreements with generative AI platforms Experience at a major publisher, record label, or digital service provider An understanding of music publishing and rights flow, particularly in the digital landscape Familiarity with the international society network (e.g., ASCAP, BMI, PRS, SACEM, etc) Ability to design high-quality decks and visual materials using presentation platforms, such as Canva or Google Slides. Your role: The Senior Director, Digital Legal Affairs, is responsible for drafting and negotiating digital license agreements with new and existing digital partners (e.g., subscription streaming, ad-supported streaming, social media platforms, services at the intersection of music and AI, gaming, fitness, and other emerging technologies), creating new licensing schemes to offer flexibility to digital partners and new opportunities for WCM songwriters, and advising on international legal and regulatory affairs that may impact the business.

30+ days ago

Buffalo, NY

$80,000–$85,000 / year

Teach in the program (as needed and aligned with expertise) and participate in curriculum review cycles, Support institutional assessment processes as related to the program (reports, data requests, and quality initiatives), Represent the program at professional meetings and build visibility within the behavior analytics education community, In coordination with the Office of Sponsored Programs & Research, support grant development and philanthropic/workforce partnership opportunities to advance simulation, scholarships, and clinical expansion, Perform other duties as assigned in support of program and university priorities. Prior role as program director, assistant/associate program director, clinical coordinator, or comparable academic leadership position in behavior analysis or related disciplines, Evidence of success in advancing student outcomes, certification exam preparedness, and post-graduation employment placement.

30+ days ago

Buffalo, NY

$80,000–$85,000 / year

Teach in the program (as needed and aligned with expertise) and participate in curriculum review cycles, Support institutional accreditation and assessment processes as related to the program (reports, data requests, and quality initiatives), Represent the program at professional meetings and build visibility within the perfusion education community (e.g., relationships consistent with how AC-PE interfaces with sponsoring organizations), In coordination with the Office of Sponsored Programs & Research, support grant development and philanthropic/workforce partnership opportunities to advance simulation, scholarships, and clinical expansion, Perform other duties as assigned in support of program and university priorities. Experience working with or leading CAAHEP-accredited allied health programs and/or direct experience preparing for CAAHEP/AC-PE accreditation review, Prior role as program director, assistant/associate program director, clinical coordinator, or comparable leadership role in perfusion education, Evidence of success with student outcomes and professional certification readiness initiatives (aligned with common perfusion program outcome expectations).

30+ days ago

Stony Brook, NY

$142,800–$203,597 / year

2602444'',''2602444'',''TH Senior Staff Associate'',''TH Senior Staff Associate'',''Clinical Management'',''Clinical Management'',''US-NY-Stony Brook'',''US-NY-Stony Brook'',''JC Continued Readiness'',''JC Continued Readiness'',''Full-time'',''Full-time'',''Day Shift'',''Day Shift'',''8:30-5'',''8:30-5'',''Sat, Sun'',''Sat, Sun'',''Jul 2, 2026'',''Jul 2, 2026'',''Oct 1, 2026, 3:59:00 AM'',''Oct 1, 2026, 3:59:00 AM'',''142800 - 203597'',''142800 - 203597'','''','''',''SL5'',''SL5'',''Stony Brook University Hospital'',''Stony Brook University Hospital'',''false'',''736662'',''736662'',''true'',''736662'',''false'',''Submission for the position: Director of Regulatory and Patient Safety - (Job Number: 2602444)'',''false'',''736662'',''false'',''true''. The department will utilize the Director''s expertise to help prioritize projects, to develop detailed project plans for major safety & regulatory initiatives, assist other members of the department in planning projects, and assure a structured, well-planned approach for successful outcomes & project completion.

1 day ago

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Director Of Regulatory Affairs Jobs in New York

Director / Senior Director of Regulatory Affairs Pathos

Executive Director, Regulatory Affairs - Global Regulatory Leader Summit Therapeutics Inc

Director, Commercial Regulatory Affairs, Labeling, Advertising, and Promotion Syndax Pharmaceuticals

Associate Director, Regulatory Affairs Recursion Pharmaceuticals Inc

Associate Director, Regulatory Affairs BeOne Medicines AG

Director, Commercial Regulatory Affairs, Labeling, Advertising, and Promotion Syndax Pharmaceuticals Inc

Director, Regulatory Affairs Nektar Therapeutics

Associate Director, CMC Regulatory Affairs Recursion Pharmaceuticals Inc

Senior Director, Clinical Regulatory Affairs Umoja BioPharma Inc

Associate Director, CMC Regulatory Affairs (Hematology/Oncology) Regeneron Pharmaceuticals Inc

Associate Director, Regulatory Affairs Nuvation Bio, Inc.

Director, Regulatory Affairs Strategy - Genetics Medicine Regeneron Pharmaceuticals Inc

Senior Director Regulatory Affairs, CMC BeOne Medicines AG

Associate Director, Regulatory Affairs, CMC BeOne Medicines AG

Regulatory Affairs Director - Hybrid (Bronx Office) CareSource

Director - Compliance Coordination and Regulatory Affairs Credit Agricole SA

Director, Global Regulatory Affairs Protara Therapeutics Inc

Director, Regulatory & Administrative Affairs - Institute for Transformative Clinical Trials Mount Sinai Health System

Senior Director/VP of Medical Affairs Click Therapeutics Inc

Manager, Regulatory Affairs, Advertising & Promotion Regeneron Pharmaceuticals Inc

Senior Director, Medical Affairs Cellectis

Quality Assurance and Regulatory Affairs Specialist EMED Technologies

Regional Government Affairs Director - Northeast Modivcare

Executive Director, EaR Strategy & Alignment, Public Affairs College Board

Senior Director, Medical Affairs Cellectis SA

Regional Government Affairs Director - Northeast ModivCare Inc.

Senior Analyst, Regulatory Affairs Oscar Health

Senior Analyst, Regulatory Affairs Oscar Health Inc

Pharmacist - Pharmacy Services/Regulatory Affairs Pine Pharmaceuticals LLC

Senior Medical Director, Medical Affairs, MASH Regeneron Pharmaceuticals Inc

Director, Influencer Marketing (Public Affairs) Orchestra

Associate Director, State Government Affairs - Remote Agios Pharmaceuticals

Manager/Director Board Governance & Executive Affairs the fedcap group

Senior Director, Medical Affairs Mineralys Therapeutics Inc

Associate Director, Field Medical Affairs- Allergy (eastern states) Regeneron Pharmaceuticals Inc

Senior Director/VP, Medical Affairs Click Therapeutics

Executive Director Global Medical Affairs, Hematology BeOne Medicines AG

Senior Director, Medical Affairs Formation Bio Inc

Vice Dean of Academic Affairs, Lewyt College of Veterinary Medicine Long Island University

Senior Director, Scientific Affairs ACM Global Central Laboratory Ltd

Senior Director, Scientific Affairs Rochester Regional Health System

Biostatistics Director, Medical Affairs BridgeBio Pharma Inc

Director, Medical Affairs Team - Internal Medicine Dechra Pharmaceuticals Ltd

Associate Director, Global Field Medical Training & Excellence - Global Medical Affairs Biogen Inc

Associate Director, AI Enablement (Commercial & Medical Affairs) BeOne Medicines AG

Senior Director, Digital Legal Affairs Warner Music Group Corp

Academic Affairs - Behavior Analyst Program Director D'Youville University

Academic Affairs - Cardiovascular/Clinical Perfusion, Program Director D'Youville University

Director of Regulatory and Patient Safety Stony Brook University

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