131 Results for

Strategic Planning Jobs in New York

Jobs

Manager, U.S. Regional Regulatory Lead - LCM CSL Plasma

Waltham, Massachusetts

$129,000–$153,000 / year

Regulatory leaders who leverage regional regulatory experience to actively contribute to an innovative, scientifically sound, global, integrated regulatory vision/strategies for assigned product/s with a patient-centric focus, leveraging regional commercial insights and applying prudent risk-taking to ensure timely delivery of successful regulatory outcomes. Developing regional knowledge regarding health authority requirements, regulatory filing pathway/categories, processes, and ways of working and thus, can provide relevant guidance / assessment to internal stakeholders (e.g., GRAST, GRL & Commercial) on means to address project challenges, leverage regulatory opportunities and advise on risk for developmental, new, and marketed products.

12 days ago

Associate Director, Corporate Communications Disc Medicine Inc

massachusetts, MA

$173,000–$212,000 / year

As Disc prepares for and executes its first drug launch, this role will also support communications related to product launch and commercialization, including coordination of launch messaging, alignment of corporate and product narratives, and collaboration with commercial, medical, and regulatory teams to ensure accurate, compliant, and impactful communications throughout the launch lifecycle. Working cross-functionally with leadership and internal stakeholders, they will ensure Disc's narrative resonates with diverse audiences-ranging from media, investors, employees, and partners to patients and the broader healthcare community.

30+ days ago

Senior Director, Regulatory Affairs CMC – Biologics Beeline Medicines

Cambridge, Massachusetts

$242,000–$313,500 / year

Demonstrate entrepreneurial drive and resourcefulness in executing CMC regulatory responsibilities — proactively seek out information, build relationships across the CMC organization, and find creative avenues to get things done; a successful CMC regulatory lead takes ownership of being plugged in, earns trust within the team, and removes barriers through initiative and ownership. Act as a fully integrated partner within the CMC team, attending key technical meetings, engaging daily with Process Development, Analytical, Manufacturing Sciences, Drug Supply and Quality colleagues, and translating regulatory strategy into practical guidance that enables the CMC team to make informed decisions and move programs forward with regulatory confidence.

9 days ago

Senior Manager, Quality Assurance Vendor & Audit Management Genetix Biotherapeutics Inc

Somerville, MA

$160,000–$180,000 / year

This role oversees the lifecycle management of suppliers, contract manufacturing organizations (CMOs), contract research organizations (CROs), laboratories, treatment centers, and other GxP service providers. The individual develops and maintains a risk-based audit strategy, drives supplier quality improvements, and supports inspection readiness across the organization.

30+ days ago

Director, Head Of Global Nemluvio Regulatory Strategy Galderma

Boston, MA

$200,000–$265,000 / year

Leads the global regulatory strategy, submission planning, and health authority engagement for Nemolizumab across all approved and development-stage indications, ensuring regulatory activities are executed in accordance with global regulatory requirements, corporate objectives, and agreed timelines. Where pay falls within the range may vary based on many factors, including, but not limited to, job responsibilities, skills, experience, education, certifications, location and applicable geographic pay zones, market conditions, internal equity and business considerations.

30+ days ago

MSAT Scientist II, Drug Product Thermo Fisher Scientific Inc

Plainville, MA

$66,000–$99,000 / year

The role works cross-functionally with Manufacturing, Process Development, Quality, Engineering, Regulatory Affairs, Supply Chain, and external manufacturing partners to ensure processes are scientifically sound, compliant, robust, and capable of consistently delivering products that meets established quality requirements. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step a step beyond by developing solutions for some of the world's toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer.

20 days ago

Associate Director, Regulatory Project Manager Relay Therapeutics, Inc.

Cambridge, MA

$150,000–$214,000 / year

You will play a key role in advancing Regulatory Project Management best practices, supporting operational excellence initiatives, and helping to build a scalable project management framework within the Regulatory function to support the company's growing portfolio. You will serve as a strategic partner to Regulatory Affairs leaders and cross-functional teams, ensuring regulatory strategies are translated into integrated, actionable plans that support successful health authority interactions and major submission milestones.

11 days ago

Regional Sales Manager, Immunology - Detroit, MI Galderma

Boston, Massachusetts

Engage in one-on-one strategic business meetings with Account Managers and HCPs, help to plan and execute sales meetings, conduct routine performance evaluations of Account Managers, and participate in company sponsored meetings. 3+ years in Sales Leadership Role; demonstrated successful history of field force management; Ability to lead and manage direct reports, establishing clear expectations, providing coaching, feedback, and assessing and evaluating performance.

12 days ago

Regional Sales Manager, Immunology - San Francisco, CA Galderma

Boston, Massachusetts

$187,000–$198,000 / year

30+ days ago

Management Consulting Supervisor, Life Sciences Advisory RSM

Boston, MA

$107,000–$214,500 / year

Responsibilities: Lead consulting engagements for Pharmaceutical and Biotechnology clients, focusing on Gross-to-Net (GTN) revenue analytics, government pricing analytics, contract and channel valuation and analysis, compliance assessments, government program and pricing operational compliance, pricing methodology development and documentation, and Fair Market Value analysis. Oversee the development, deployment, and maintenance of price modeling related to various government price points (e.g., Average Manufacturer Price, Best Price, Unit Rebate Amount, Average Sales Price, non-Federal Average Manufacturer Price) and impact analyses for commercial, government, and distribution contracts.

26 days ago

VP, Legal and Head of Regulatory Affairs - Patriot Hydro LS Power Development, LLC

Manchester, New Hampshire

Full time

Draft, review, and negotiate power purchase agreements, renewable attribute agreements, hedging and trading documents, interconnection agreements, equipment and service contracts, operations and maintenance agreements, real estate documents, easements, access agreements, confidentiality agreements, and other commercial contracts. Success will be measured by the quality and responsiveness of legal support, reliable execution of licensing and compliance obligations, constructive agency and stakeholder relationships, effective management of legal and regulatory risk, and the development of a consistent portfolio-wide legal and regulatory framework.

14 days ago

Senior Manager, Regional Regulatory Lead - US (Hematology) CSL Plasma

Waltham, Pennsylvania

$150,000–$180,000 / year

Cross-Functional Collaboration: Partner with Global Regulatory Leads, Global Regulatory Affairs Strategy Team (GRAST) members, Regulatory CMC, regional commercial operations, and other stakeholders to ensure consistent regulatory positions, informed decision-making, and effective execution of regulatory plans. The Regional Regulatory Lead (RRL) partners closely with Global Regulatory Leads (GRLs), cross-functional regulatory teams, Regulatory CMC, and commercial stakeholders to support regulatory strategy, product development, submissions, and health authority interactions.

7 days ago

Senior Advisor, Regulatory Starting Material Centessa Pharmaceuticals, LLC

Boston, MA

$140,000–$210,000 / year

Reporting to the Vice President, CMC, this role will serve as the internal and external subject matter expert on RSM selection in accordance with ICH Q11 and applicable regional guidance, ensuring synthetic routes, GMP starting points, and supply strategies are scientifically sound, regulatorily defensible, and aligned with commercial manufacturing readiness. The individual in this Associate Director level role will lead the strategy, justification, and regulatory positioning of Regulatory Starting Materials for drug substance manufacturing processes supporting late-stage clinical and commercial programs.

30+ days ago

Senior Manager, Clinical Supply Chain eTeam Inc.

Marlborough, MA

$100–$103 / hour
Quick Apply

In addition, working closely with CClient, Regulatory Affairs, Quality Assurance, Clinical Operations, and /or SMPA external partners and CMOs, as needed, building strong working relationships, support study project teams and ensure timely Investigational Product (IP) for clinical trials. JOB DESCRIPTION Responsible for managing drug supply planning, inventory control, and distribution activities including label/pack scheduling, issue resolution, change implementation, vendor oversight, and scope review related to clinical supplies on multiple clinical programs.

30+ days ago

Medical Director, Rheumatology, Global Medical Affairs Zenas BioPharma (USA) LLC

Waltham, MA

$204,000–$255,000 / year

Zenas' earlier stage programs include ZB021, a clinical-stage, potentially best-in-class, oral, IL-17AA/AF inhibitor; ZB022, a preclinical, potentially best-in-class, oral, brain-penetrant, TYK2 inhibitor; and ZB014, a preclinical half-life extended anti-CD-19 and FcRIIb monoclonal antibody. Our core business strategy combines our experienced leadership team with a disciplined product candidate acquisition approach to identify, acquire and develop product candidates globally that we believe can provide superior clinical benefits to patients living with autoimmune diseases.

7 days ago

Medical Director, Clinical Development Disc Medicine Inc

massachusetts, MA

$279,000–$341,000 / year

Reporting to the Executive/Senior Medical Director of the program, this individual will be able to work in a fast-paced environment and collaborate with cross-functional teams and external stakeholders to advance innovative therapies from early clinical development through later-stage development and regulatory evaluation. POSITION OVERVIEW: The Medical Director, Clinical Development is a key clinical leader responsible for providing medical and scientific leadership across the design, execution, and interpretation of clinical development programs supporting Disc's pipeline.

30+ days ago

Associate Director, Market Insights Disc Medicine Inc

massachusetts, MA

$173,000–$212,000 / year

Track key external and internal signals that may affect commercialization assumptions, including clinical readouts, regulatory milestones, competitive events, access dynamics, customer feedback, and market structure changes. COMPANY OVERVIEW: Disc Medicine is a clinical-stage biopharmaceutical company committed to discovering, developing, and commercializing novel treatments for patients who suffer from serious hematologic diseases.

19 days ago

Director, Global Clinical Physician (Cardiovascular) Bristol-Myers Squibb Co

$308,700–$374,075 / year

Advanced planning/project management skills (develop realistic, effective medium-range plans across clinical development programs and deal timelines, managing competing priorities across multiple concurrent deals). Based on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day.

30+ days ago

Vice President, Program Management Kailera Therapeutics

Waltham, Massachusetts

The Vice President will directly manage a team of thee Program Managers (plus additional contract Program Managers) and serve as the cross-functional connective tissue that keeps teams aligned, milestones on track, and risks visible. Collaborate with Program Leader / SVP Franchise Lead to align strategic objectives with execution plans, ensuring program teams remain focused on priorities, milestones, risks, and decision points.

30+ days ago

Medical Science Liason (MSL) - Podiatry, Men's Health and Ortho (Northeast) Mallinckrodt LLC

Boston, MA

Remote

$157,000–$186,000 / year

This is a field-based Medical Affairs position requiring a strong scientific background (technical or clinical experience) as the MSL will be a credible source of clinical/scientific data as well as technical/practical education to practicing clinicians, key opinion leaders (KOL), professional societies, and payers. A Medical Science Liaison (MSL) will serve as a liaison to the medical/scientific community and will be responsible for establishing, developing and maintaining relationships with key stakeholders within the geographic and therapeutic area of coverage.

30+ days ago

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Strategic Planning Jobs in New York

Manager, U.S. Regional Regulatory Lead - LCM CSL Plasma

Associate Director, Corporate Communications Disc Medicine Inc

Senior Director, Regulatory Affairs CMC – Biologics Beeline Medicines

Senior Manager, Quality Assurance Vendor & Audit Management Genetix Biotherapeutics Inc

Director, Head Of Global Nemluvio Regulatory Strategy Galderma

MSAT Scientist II, Drug Product Thermo Fisher Scientific Inc

Associate Director, Regulatory Project Manager Relay Therapeutics, Inc.

Regional Sales Manager, Immunology - Detroit, MI Galderma

Regional Sales Manager, Immunology - San Francisco, CA Galderma

Management Consulting Supervisor, Life Sciences Advisory RSM

VP, Legal and Head of Regulatory Affairs - Patriot Hydro LS Power Development, LLC

Senior Manager, Regional Regulatory Lead - US (Hematology) CSL Plasma

Senior Advisor, Regulatory Starting Material Centessa Pharmaceuticals, LLC

Senior Manager, Clinical Supply Chain eTeam Inc.

Medical Director, Rheumatology, Global Medical Affairs Zenas BioPharma (USA) LLC

Medical Director, Clinical Development Disc Medicine Inc

Associate Director, Market Insights Disc Medicine Inc

Director, Global Clinical Physician (Cardiovascular) Bristol-Myers Squibb Co

Vice President, Program Management Kailera Therapeutics

Medical Science Liason (MSL) - Podiatry, Men's Health and Ortho (Northeast) Mallinckrodt LLC

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