Senior Manager for Regulatory Affairs
Artech Information Systems LLC
Company DescriptionArtech Information Systems is the #1 Largest Women-Owned IT Staffing Company in the U.S. and an employer of choice for over 7,500 consultants. We recruit world-class talent for IT, engineering, and other professional jobs at 70+ Fortune and Global 500 companies coast-to-coast across the U.S., India, and China. We are one of the fastest-growing companies in the US.At the forefront of the staffing industry, Artech is a minority and women-owned business enterprise (MWBE) committed to maximizing global workforce solutions on behalf of its clients. Artech's deep heritage, proven expertise and insightful market intelligence has secured long-term partnerships with Fortune 500 and government clients seeking world-class professional resources.Job DescriptionUS Regulatory Advertising and Promotion (US Reg AD/Promo) is responsible for actively contributing to the implementation of regulatory strategy for promotional messaging. The contractor will serve as the regulatory representative on assigned review teams for promotional and non-promotional materials and contribute, as appropriate, to other assigned projects. Essential functions: • Responsible for accuracy and content of communications with FDA • Extensive knowledge of advertising and promotion regulations and ability to interpret regulations to promotional materials and non-promotional materials • Ability to influence teams • Actively contribute to the development and implementation of regulatory strategy for promotional materials as well as any other assigned projects and programs. • Decision maker in review meetings • Responsible for coordinating all aspects of regulatory submissions relevant to assigned projects and programs. This includes promotional materials, including pre-use submissions for subpart E & H products. • Provide regulatory guidance to cross-functional teams that establish strategy and vision for promotional materials, sales training materials, and other external communications. • Work is performed under general direction. Capable of strategic thinking and risk assessment for area of responsibility. Demonstrate good communication skills (oral/written/listening). QualificationsRequires a minimum of 5+ yrs of direct regulatory promotional and non-promotional material review experience.Additional InformationAll your information will be kept confidential according to EEO guidelines.SummaryType: ContractFunction: ManagementExperience level: Mid-Senior LevelIndustry: Pharmaceuticals
- Job Description: This role is within the Global Regulatory Affairs (GRA) Chemistry Manufacturing & Controls (CMC) and Devices organization... ...will contribute: With some supervision, plans, executes and manages regulatory submissions according to the regulatory strategy...Senior
$145k - $215k
...inclusivity, so that our people are valued, seen, and heard.How you’ll make an impact:Kymera Therapeutics is seeking a Senior Manager, Regulatory Affairs to serve as a key regulatory contributor and emerging strategic leader across multiple drug development programs....Senior$137k - $215.27k
...therapies to patients worldwide.This role is within the Global Regulatory Affairs (GRA) Chemistry Manufacturing & Controls (CMC) and Devices... ...will contribute:With some supervision, plans, executes and manages regulatory submissions according to the regulatory strategy...SeniorMinimum wageTemporary workLocal areaRemote workWorldwide$270k - $350k
...The Senior Director, Regulatory Affairs is responsible for planning, developing, and implementing regulatory strategy, submissions, and compliance... ...appropriate manner across global markets. Independently manage the development of high-quality regulatory documents, including...SeniorShift work- Senior Regulatory Affairs Manager- REMOTE I'm looking for a senior manager, regulatory affairs to lead our growing, dynamic team through global phase 3 clinical trials of a certain product and support other clinical studies. This role includes driving global submission...SeniorFull timeRemote work
- The Global Regulatory Affairs (GRA) is responsible for obtaining approval for new products and ensuring that approval is maintained throughout... ...AD will typically collaborate, influence and negotiate with senior Nonclinical / Clinical leaders on product strategies and actions...Senior
$275k - $315k
...OverviewBicara Therapeutics is seeking a strategic and experienced Senior Director of Regulatory Affairs to lead and execute US regulatory strategy for our... ...—from IND through BLA submission and approval. You will manage a small team of Regulatory Affairs professionals,...SeniorFull timeTemporary workWork at officeLocal area3 days per week- ...is a Boston-based biopharmaceutical company seeking a Senior Director, US Regional Regulatory Lead to shape US regulatory strategy and lead FDA interactions... .... The role requires 12+ years in Regulatory Affairs, leadership experience, and a strong background in oncology...SeniorRemote work
- ...EMD Serono, Inc. is seeking a Senior Director to lead a team in regulatory review of promotional materials for U.S. prescription drugs. This role ensures compliance with FDA regulations and shapes the regulatory strategy across multiple therapeutic areas. The ideal candidate...Senior
- ...visit us at . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. Job Description The Senior Manager Regulatory Affairs, Chemistry, Manufacturing and Controls (CMC) works with internal and external partners to deliver products to patients...SeniorFull timeWork at officeLocal areaRemote work
- ...years professional experience in legal, regulatory, compliance environments; attorneys with... ...preferred5+ years in end-to-end allegations management programs including intake/triage, case... ...trust-based relationships with senior leaders within and outside of the team;...SeniorApprenticeshipWork at office
- ...Chemistry, Manufacturing and Controls (CMC) regulatory strategy for development and lifecycle... ...or train staff; may have direct line management responsibility. Manage project activities... ...professional growth in global regulatory affairs, including communication of evolving/...SeniorWork at officeLocal areaRemote workWorldwide
$163.5k - $281.6k
...strengthen how health is understood and managed, and support the communities we serve. This... ...and implement comprehensive global regulatory CMC strategies for assigned gene therapy... ...providing strategic recommendations to senior leadership. Stay current with evolving global...SeniorFull timeFor contractorsWork at officeFlexible hours$200k - $220k
...Director/ Senior Director, Regulatory CMC Join Us in Tackling Autoimmune Disease at Its Root At Vor, we believe science can do more than manage symptoms. It can change the course of disease. By advancing telitacicept, a first‑and potentially best‑in‑class dual BAFF/APRIL...SeniorContract workWorldwideFlexible hours$183.55k - $275.32k
...Director/Sr. Director, Regulatory Labeling Strategy, Advertising, and... ...approval of labeling documents. Manage the creation and/or... ...Act as a trusted advisor to senior leadership on promotional risk... ...of experience in Regulatory Affairs within the biopharmaceutical...SeniorTemporary workLocal areaRemote workWork from homeFlexible hours3 days per week$220k - $290k
...therapy in the U.S. and are exploring regulatory pathways for Europe and Japan. We... ...regulatory barriers, and identify and manage potential risks. Act as primary... ...Corporation’s short and long‑term plans. The Senior Director, Regulatory Affairs has foresight, is action oriented, a...SeniorTemporary workFor contractorsWork at officeWeekday work$238k - $294k
...Sr. Director, Regulatory Labeling and Advertising Promotion About Genetix... ...Development, Medical Affairs, Commercial, Legal, and Safety... ...labeling strategy, lifecycle management, and promotional material review... ...and partner effectively with senior leaders. Strong attention to...SeniorFull timeWork at officeFlexible hours3 days per week$242k - $313.5k
...mediated diseases can live life fully. Job Summary The Senior Director, Regulatory Affairs CMC – Biologics provides senior‑level scientific and strategic... ...through BLA filing and post‑approval lifecycle management, serving as the company's foremost authority on biologics...SeniorLocal areaFlexible hours2 days per week$232k - $348k
Job DescriptionThe Regulatory Strategy Senior Director is a regulatory leader with expert technical and tactical experience... ...and GRA leadership. Counsels and advises senior management on status of global Regulatory Affairs strategies and tactics, procedures and practicesLeads...SeniorFull timeSummer workWork at officeLocal areaRemote workFlexible hours2 days per week3 days per week$218.06k - $327.09k
Job Title: Senior Director, Regulatory Affairs Strategy - Cell Therapy Available locations: Gaithersburg, MDBoston, MASouth San Francisco, CASanta... ...enable decisive, data-driven choices.Delivery and Milestone Management: Oversee all regulatory deliverables and milestones,...SeniorHourly payFull timeTemporary workStart working todayWork at officeFlexible hours3 days per week- ...kJob Description An established organization is seeking a Senior Compliance Manager to support and drive compliance initiatives across regulated... ...systems, and operations align with industry standards and regulatory requirements. This hands on position partners with cross...SeniorFlexible hours
$240k - $320k
...impact.The OpportunityThis role leads US regulatory policy and advocacy efforts to support the advancement and lifecycle management of Galderma portfolio. The position plays... ...Liaise with other GRA staff, US government affairs staff, R&D functions, and other internal stakeholders...SeniorFull timeTemporary workWork experience placementWork at officeWorldwide- ...EY is seeking a Senior Manager for its Life Sciences Regulatory Submissions practice based in Boston. This role focuses on driving growth and establishing EY as a leader in regulatory compliance. The ideal candidate will have extensive experience in regulatory submissions...Senior
- ...A medical device company in Cambridge, MA, is seeking a Regulatory Affairs professional to lead regulatory strategies for Class II medical devices. Responsibilities include managing FDA submissions, ensuring regulatory compliance throughout product development, and collaborating...Senior
$212k - $333.19k
...patients worldwide.Join Takeda as a Senior Director, Global Regulatory Lead - Oncology, where you will be part... ...functional stakeholders and senior management.Acts independently under the... ...understanding broad concepts within regulatory affairs and implications across the...SeniorMinimum wageTemporary workLocal areaRemote workWorldwide$116k - $160k
Job DescriptionWe are seeking an experienced regulatory professional to support global regulatory activities across early... ...late-stage development programs through lifecycle management. The Manager, Regulatory Affairs will partner cross-functionally to support high-...$272.57k - $327.09k
...your development at every step. The Senior Director, Global Regulatory Strategy will be responsible for providing... ...registration and lifecycle management of unique and technologically complex... ...(e.g. Clinical, Commercial, Medical Affairs, amongst others) to provide regional...SeniorTemporary workWork at office3 days per week$251.77k - $307.72k
...experienced QMS and Digital Compliance Senior Director to lead transformational change... ...functional partnerships, maturing the quality management system and digital compliance footprint... ...framework ensuring compliance with regulatory requirements, industry standards, and company...SeniorFull time$170k - $240k
Litigation Marketing Senior Manager - RegulatoryCooley is seeking a Litigation Marketing Senior Manager - Regulatory to join the Marketing team.Position summary: The Senior Practice Group Marketing Manager leads the marketing and client development activities for assigned...SeniorFull timeTemporary workWork at officeImmediate startFlexible hoursWeekend work$250k - $280k
...growth, product lifecycle, and market expansion. Serve as the accountable Compliance & Ethics business partner for Commercial, Medical Affairs, Patient Services, and Patient Advocacy. Represent Compliance in cross-functional leadership discussions and embed compliance into...Senior
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