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
- ...Reference26-00886 Job Description: 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...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$259k - $317k
...in the lives of patients we serve.Position Summary:The Senior Director of Regulatory Affairs is a senior leader responsible for developing and executing... ...authoring and reviewing Module 2 summaries and managing cross-functional submission teamsOversee preparation, review...SeniorFull timeWork at officeFlexible hours$134k - $149k
We are seeking an individual who is talented, motivated, and passionate about science to join our Regulatory Strategy team. As Senior Manager of Regulatory Affairs, the successful candidate will play an important role in guiding new products into the clinic and setting...SeniorWork at officeLocal areaFlexible hours3 days per week- ...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
$270k - $350k
The Senior Director, Regulatory Affairs is responsible for planning, developing, and implementing regulatory strategy, submissions, and compliance activities... ...manner across global markets. Independently manage the development of high-quality regulatory documents, including...SeniorShift work- Job-ID31521196Reference25-04484 The Global Regulatory Affairs (GRA) is responsible for obtaining approval for new products and ensuring that... ...AD will typically collaborate, influence and negotiate with senior Nonclinical / Clinical leaders on product strategies and actions...Senior
$233k - $280k
...Dyne advances toward launch. Acting as a senior strategic and operational partner to the... ...Operations & Operating Rhythm: Establish and manage the operating rhythm for the Commercial... ...in partnership with Corporate Affairs.Help strengthen Commercial team culture by...SeniorFull timeWork at officeLocal area$172.5k - $222.5k
...where new ideas are encouraged and everyone is a stakeholder.What you’ll be responsible for: Circle is looking for a Senior Manager to join the Regulatory Assurance team who will help to create a central global function focused on developing a best in class compliance...SeniorFlexible hours- ...about AbbVie, please visit us at Follow @abbvie on LinkedIn, Facebook, Instagram, X and YouTube. Job Description The Senior Manager, Regulatory Affairs US & Canada Strategy Lead - Therapeutic Neurotoxins is responsible for the development and implementation of US and...SeniorLocal area
$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- ...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
$195k - $330k
...development and execution of global regulatory CMC strategies for degrader... ...regulatory CMC guidance to senior leadership regarding health... ...and lead the Regulatory Affairs CMC function as the pipeline... ...control strategy, and lifecycle management.Demonstrated success independently...Senior- Genetix Biotherapeutics is seeking a Sr. Director, Regulatory Affairs in Boston to lead regulatory activities for product labeling and U.S. advertising compliance. The candidate will ensure that all materials are compliant, meet scientific standards, and align with corporate...SeniorFull time
$196.7k - $353.4k
...seeking an individual to lead development and execution of global regulatory strategy for programs in its oncology portfolio. This leader... ...external to the company Demonstrated competence in employee management and development Knowledge of and broad experience with regulatory...SeniorPermanent employmentFull timeWork at officeWork from home- ...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
$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- ...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
- Title: Director / Senior Director, Global Regulatory Lead Location: San Francisco, CA or Boston, MA -> hybrid 3-days per week (relocation offered!... ...degree (PhD, PharmD, MS) preferred 10+ years of regulatory affairs experience within biotech/pharma Recent, hands-on...SeniorRelocation3 days per week
- ...Senior Director, IT Compliance & Governance (Contractor) About the Company Innovative company designing & developing gene therapeutic... ...successful candidate will be responsible for the operational management of GxP Compliance Audit and Supplier Quality Management...SeniorFor contractors
- Senior Manager - Regulatory Affairs Operations Location - Cambridge, MA (Hybrid) Oncology Biotech | Global Clinical Programs I’m currently supporting an innovative clinical-stage biotechnology company developing next-generation therapies in oncology. With multiple clinical...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
...dependent care. Job DescriptionWe are seeking an experienced regulatory professional to support global regulatory activities... ...late-stage development programs through lifecycle management. The Manager, Regulatory Affairs will partner cross-functionally to support high-...Flexible hours$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- ...accepted standards like GxP, ISO 9001, and 21 CFR Part 11. As Senior Compliance Manager, US, you will operate as an independent senior IC —... ...for ensuring TetraScience's products and platform meet the regulatory expectations of the world's largest pharma and biotech customers...SeniorImmediate startFlexible hours
- The J.Jill Group is seeking an Import Compliance professional to strengthen the intake controls for U.S. imports and to verify supplier adherence to J.Jill’s ethical standards. You will support the Director on ongoing compliance projects and help ensure cost-effective, ...Senior
$167k - $300.7k
...The Role Moderna, Inc. is seeking a Director of Regulatory Strategy to support select programs within the rare, autoimmune and oncology... ...Science Leadership Team, Project Development Team and senior management, as relevant. Collaborates with internal teams and Moderna partners...SeniorPermanent employmentWork at officeWork from home- ...responsible for the design, implementation and ongoing management of a sophisticated private credit compliance... ...advising on co-investments, affiliated transactions, and regulatory considerations while reporting to senior leadership and the board. #J-18808-Ljbffr Origin...Senior
- PharmaEssentia USA Corporation seeks a Director of Regulatory Advertising & Promotion to lead compliance across advertising and promotional activities. You will oversee cross-functional governance, ensure scientific accuracy aligned with labeling, and drive submission...Senior
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