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📑 1123 open jobs. Use your resume to get matched with the right job. Upload your resume Vice President – Public Policy and Government Affairs Washington, DC, United States and 1 more LA-Legal Director, Managing Counsel-Regulatory Policy / Market Structure – Public Policy and Government Affairs Washington, DC, United States and 1 more LA-Legal ...

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📑 Nanobiotix – a brief historyEst. 2003, Nanobiotix is a clinical-stage biotechnology company focused on developing first-in-class product candidates that use proprietary nanotechnology to transform cancer treatment.Headquartered in Paris (c.70 staff) and with a US affiliate in Cambridge, MA (c.20 staff),Nanobiotix designs and manufactures nanopartic ...

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📑 About the RoleThe Associate Director, US Regulatory Affairs (RA) serves as the regulatory lead on relative Review Committees (RCs), for products in the Rare Disease, Rare Blood Disorder and Neurology portfolio. As the RC RA representative, work with brands on competitively positioning assigned products appropriately while maintaining compliance wit ...

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📑 OPEN JOB: Pharma - Associate Director , US Advertising and Promotion , Global Regulatory Affairs - Hybrid LOCATIONS: this is a hybrid role based in either Bridgwater, NJ or Cambridge, MA. Hybrid work arrangement. Candidate must be in office 2-3x/week at either Bridgewater NJ or Cambridge MA location. TARGET COMP: $150,000 to $175,000 Candi ...

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📑 OPEN JOB: Pharma - Associate Director , US Advertising and Promotion , Global Regulatory Affairs - Hybrid LOCATIONS: this is a hybrid role based in either Bridgwater, NJ or Cambridge, MA. Hybrid work arrangement. Candidate must be in office 2-3x/week at either Bridgewater NJ or Cambridge MA location. TARGET COMP: $150,000 to $175,000 Candi ...

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📑 Description We're looking for an Associate Director of Regulatory Affairs, working in Pharmaceuticals and Medical Products industry in Cambridge, Massachusetts, United States. Works proactively in a cross-functional organization to partner with various other expertise areas and regional regulatory partners (as applicable) to plan and execute ...

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📑 Regulatory Affairs Expert-Medical Devices1 Year (Extendable & potential to convert) St Louis, MOMax PR: $25-33/hr Your Role:With minimal supervision, the Regulatory Affairs Expert-Medical Devices manages assigned regulatory tasks related to health authority notifications, submissions, and registrations regarding renewals and new products, and chang ...

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📑 Title: Regulatory Affairs Associate Location: New Jersey (ONSITE) Job Type: 12-Month Contract Start Date: ASAP Reputable pharmaceutical client is seeking a Regulatory Affairs Associate to join their Regulatory Affairs team on a long-term contract. The ideal candidate will have 1-3 years of experience, hands-on experience with publishing submissions ...

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📑 Description We're looking for an Associate Director Regulatory Affairs CMC, working in Pharmaceuticals and Medical Products industry in Cambridge, Massachusetts, United States. Leads development and execution of robust global regulatory CMC strategy for assigned program(s) with balanced risk-based approach using scientific rationale and in a ...

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📑 Associate Director/Director, Regulatory Affairs (Oncology)Remote - East Coast CandidatesMeet has partnered with a very well-established pharma with roughly 20 approved products and a robust development pipeline. They are looking for an Associate Director or Director of Regulatory Strategy to join their team. This role will be reporting into the VP ...

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📑 NEW - Regulatory Affairs Associate Director (Strategy) - Top PharmaRemote EST, however, if within 1-hour of office, hybrid model (2-3x days a week on-site) is required. Company Overview:We are excited to partner with a leading pharmaceutical company dedicated to improving global health through innovative medicines. They are committed to developing ...

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📑 Corporate Counsel, US Market Access Legal page is loaded Corporate Counsel, US Market Access Legal Bewerben locations Bridgewater, NJ Cambridge, MA time type Vollzeit posted on Vor 3 Tagen ausgeschrieben job requisition id R2732418 Corporate Counsel, US Market Access LegalDescription:We are seeking an experience ...

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📑 A leading biotechnology firm specializing in dermatology research and development is looking for an Associate Director, Regulatory Affairs. Position Summary: The Associate Director of Regulatory Affairs will play a pivotal role in driving regulatory strategy and execution for our dermatology-focused biotech initiatives. Reporting to the Director of ...

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📑 NEW - Regulatory Affairs Associate Director (Strategy) - Top PharmaRemote EST, however, if within 1-hour of office, hybrid model (2-3x days a week on-site) is required. Company Overview:We are excited to partner with a leading pharmaceutical company dedicated to improving global health through innovative medicines. They are committed to developing ...

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📑 A leading biotechnology firm specializing in dermatology research and development is looking for an Associate Director, Regulatory Affairs. Position Summary: The Associate Director of Regulatory Affairs will play a pivotal role in driving regulatory strategy and execution for our dermatology-focused biotech initiatives. Reporting to the Director of ...

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📑 US Medical Science Liaison, Immunology - Non-Alliance - GI/RESP - • Western PA, Upstate NY, RI, MA, NH, VT, ME page is loaded US Medical Science Liaison, Immunology - Non-Alliance - GI/RESP - • Western PA, Upstate NY, RI, MA, NH, VT, ME Bewerben locations Cambridge, MA time type Vollzeit posted on Gestern ausge ...

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📑 Associate Director, Regulatory Affairs, Advertising & Promotion—New JerseyTanner and Associates is recruiting an Associate Director, Regulatory Affairs, Advertising & Promotion for a Pharmaceutical Company. This Job is located in New Jersey. Responsibilities: Provides strategic and operational leadership in advertising and promotion for the US mark ...

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📑 Meets clinical-stage biopharmaceutical client based in the Bay Area is seeking a highly motivated individual to join their growing regulatory affairs group. The Associate Director / Director, Regulatory Affairs will work closely with the Regulatory Affairs team and other departments to develop and implement regulatory strategies for the company's r ...

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📑 The Genmab Vacancy Website is hosted by our Global HR System vendor, Workday. If you have any questions related to the hosting of this site please contact us at Workday@Genmab.com . Associate Director, Global Regulatory Affairs CMC page is loaded Associate Director, Global Regulatory Affairs CMC Apply locations Copenhagen ti ...

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📑 Apply now and our proprietary system will quickly have you in front of a live recruiter. The Opportunity Description We're looking for an Associate Director Regulatory Affairs CMC, working in Pharmaceuticals and Medical Products industry in Cambridge, Massachusetts, United States. Leads development and execution of robust global regulatory CMC st ...

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📑 Associate Director, Global Regulatory Affairs - Early-Development ** Rare Diseases ** PIP's and ODD's** Boston, MAWe have a new RA Associate Director position with a Greater Boston-based Rare Disease Biotech, which is well-funded with a broad portfolio of TA's and indications across a variety of modalities who are led by a talented and highly regar ...

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📑 Description We're looking for a Manager of Regulatory Affairs, working in Biotechnology/Medical Devices industry in Cambridge, Massachusetts, United States. Works with Regulatory Affairs management to define regulatory strategy and to compile and submit, in a timely manner, regulatory documents according to regulatory requirements.Develops det ...

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📑 We are partnering with a growing biotech that is seeking a highly skilled and experienced Associate Director of Regulatory Affairs Strategy to join our Regulatory Affairs team. The successful candidate will play a pivotal role in developing and executing regulatory strategies to support the successful development, registration, and commercializatio ...

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📑 We are partnering with a growing biotech that is seeking a highly skilled and experienced Associate Director of Regulatory Affairs Strategy to join their Regulatory Affairs team. The successful candidate will play a pivotal role in developing and executing regulatory strategies to support the successful development, registration, and commercializat ...

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📑 A Pharmaceutical business in New Jersey is looking for an Associate Director, Regulatory Affairs to join their Global team. In this role you will serve as the regulatory lead on relative Review Committees, for products in the Rare Disease, Rare Blood Disorders and the companies Neurology portfolio.Responsibilities:Represents Global Regulatory Affai ...

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📑 Manager, Regulatory Affairs page is loaded Manager, Regulatory Affairs Apply locations Anchorage, Alaska time type Full time posted on Posted 30+ Days Ago job requisition id JR100071 It's fun to work in a company where people truly BELIEVE in what they're doing! We're committed to bringing passi ...

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📑 Overview At the heart of QIAGEN’s business is a vision to make improvements in life possible. We are on an exciting mission to make a real difference in science and healthcare. We are still the entrepreneurial company we started out as and have today achieved a size where we can bring our full power to many ...

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📑 If you are unable to complete this application due to a disability, contact this employer to ask for an accommodation or an alternative application process. Associate Director, Regulatory Affairs CMC Full Time Mgr & Dir - R&D/Ops Malvern, PA, US 10 days ago Requisition ID: 1072 The Associate Director, Regulatory Affairs CMC will le ...

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📑 Associate Director, Regulatory AffairsThis position will serve as the company US Agent and a contact point between the FDA and company sites. Responsible to communicate with FDA for all regulatory issues/questions and provide regulatory guidance to internal constituents. It will lead a team of Regulatory Associates and Senior Regulatory Associates ...

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📑 Associate Director, Regulatory AffairsThis position will serve as the company US Agent and a contact point between the FDA and company sites. Responsible to communicate with FDA for all regulatory issues/questions and provide regulatory guidance to internal constituents. It will lead a team of Regulatory Associates and Senior Regulatory Associates ...

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📑 Overview:Lupin is comprised of a fast growing, innovative and robust team of manufacturing, Research and Development and commercial divisions. Together these entities make up the generic and branded U.S. business. Lupin has a significant generic pipeline, and a branded focus on womens health. Our first Research and Development facility in the US ...

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📑 As an Associate Director, Field Medical Affairs, you will play a pivotal role as a field-based, medical science liaison with Ophthalmology expertise. We deliver strategic and operational support by establishing, developing, maintaining scientific exchange with medical specialists, health care professionals, and payers. Additionally, we particip ...

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📑 The Newell group assisting a rapidly-growing med device/biomed company in San Antonio as they search for their nextEngineering Manager to help with their mission of developing and manufacturing current and emerging class i and ii med devices. We are looking to visit with candidates who haveBachelor's or better in Biomedical Engineering or simil ...

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📑 Why Endo?We want the best and brightest people at Endo to help us achieve our mission to develop and deliver life-enhancing products through focused execution. Our nearly 3,000 global team members understand the important role we play in delivering healthcare and are dedicated to supporting each other as we work to bring the best treatments forward ...

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📑 The Associate Director of Regulatory Affairs CMC will be responsible for developing, implementing and advising on global Regulatory CMC strategies for new and late stage programs to secure approval of the manufacturing process and control testing for initial clinical trials under INDs/CTAs and transition to appropriate GMP validation to move expedi ...

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📑 Title: Senior Medical Director, Clinical DevelopmentDescription: The Senior Medical Director, Clinical Development is a vital contributor to clinical development programs, overseeing study-specific activities, collaborating with cross-functional teams, and supporting regulatory activities. Responsibilities include protocol design, data analysis, co ...

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📑 Associate Director, Regulatory Affairs Vendor Management (Boston, MA) page is loaded Associate Director, Regulatory Affairs Vendor Management (Boston, MA) Apply locations Boston, MA time type Full time posted on Posted 4 Days Ago job requisition id REQ-21258 Job DescriptionGeneral Summary:The Vendor Management As ...

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📑 All Jobs > Associate Director of CMC Regulatory Affairs Associate Director of CMC Regulatory Affairs Fully Remote • US Remote - WA, NM, SD, KS, TX, IN, SC, NC, PA, NY, or MA applicants only Description JOB TITLE: Associate Director of CMC Regulatory AffairsLOCATION: The role is remote in the USA, but only eligible to residents of the ...

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📑 Vice President, Global Program Lead Neuroscience page is loaded Vice President, Global Program Lead Neuroscience Apply locations Princeton - NJ - US Cambridge Crossing - MA - US time type Full time posted on Posted 2 Days Ago job requisition id R1578733 Working with UsChallenging. Meaningful. Li ...

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📑 Sr Medical Director, Thoracic Oncology, US Medical Affairs Oncology, MD page is loaded Sr Medical Director, Thoracic Oncology, US Medical Affairs Oncology, MD Apply locations United States - New York - New York City United States - California - La Jolla United States - Washington – Bothell United States - Pennsylvania - Collegeville ...

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📑 The Genmab Vacancy Website is hosted by our Global HR System vendor, Workday. If you have any questions related to the hosting of this site please contact us at Workday@Genmab.com . Associate Director/Senior Manager, Global Regulatory Affairs Project Lead page is loaded Associate Director/Senior Manager, Global Regulatory Affairs Project ...

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📑 BioPhase specializes in recruiting top talented professionals for the San Diego County Scientific community. We are currently looking for a hybrid (3 days/week in-office) Associate Director of Regulatory Labeling to work for a leading San Diego biopharma company.*Must be local to San Diego, CA in a hybrid capacityKey Responsibilities:Develop draft ...

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📑 BioPhase specializes in recruiting top talented professionals for the San Diego County Scientific community. We are currently looking for a hybrid (3 days/week in-office) Associate Director of Regulatory Labeling to work for a leading San Diego biopharma company.*Must be local to San Diego, CA in a hybrid capacityKey Responsibilities:Develop draft ...

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📑 Associate Director, Regulatory LabelingRemote for East Coast CandidatesMeet has partnered with a very well-established pharma with roughly 20 approved products and a robust development pipeline. They are looking for an Associate Director of Regulatory Labeling to support their P3/commercial products. This position will be collaborating heavily with ...

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📑 Associate Director, Regulatory LabelingRemote for East Coast CandidatesMeet has partnered with a very well-established pharma with roughly 20 approved products and a robust development pipeline. They are looking for an Associate Director of Regulatory Labeling to support their P3/commercial products. This position will be collaborating heavily with ...

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📑 Regulatory Affairs Expert-Medical Devices1 Year (Temp to perm) St Louis, MO (Hybrid 2-3 days onsite)Pay: $33.00/hr Your Role:With minimal supervision, the Regulatory Affairs Expert-Medical Devices manages assigned regulatory tasks related to health authority notifications, submissions, and registrations regarding renewals and new products, and chan ...

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📑 Job Title : Manager/Associate Director, Health Economics and Outcomes Research (HEOR)Location: 100% Remote Duration: 12 Months Candidate Requirements: s MS or PhD in Health economics, Pharmacoeconomics, health services research, public health or related field. s Experience with development and execution of economic modeling strategies s Experience ...

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📑 Bausch + Lomb (NYSE/TSX: BLCO) is a leading global eye health company dedicated to protecting and enhancing the gift of sight for millions of people around the world—from the moment of birth through every phase of life. Our mission is simple, yet powerful: helping you see better, to live better. Our comprehensive portfolio of over 400 products is ...

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📑 McKesson is an impact-driven, Fortune 10 company that touches virtually every aspect of healthcare. We are known for delivering insights, products, and services that make quality care more accessible and affordable. Here, we focus on the health, happiness, and well-being of you and those we serve - we care. What you do at McKesson matters. We foste ...

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📑 The CompanyOur client is a California Biotech working on immunology and oncology products.The RoleThey are looking for a Regulatory Affairs contractor for 10 hrs a week, who will be responsible for aiding and working in a fast pace accelerated environment.This is a remote 6 month contract position, looking for 10 hr/week.Responsibilities:Assist in ...

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