📑 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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📑 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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📑 By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’s Privacy Notice and Terms of Use. I further attest that all information I submit in my employment application is true to the best of my knowledge. ...
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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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📑 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 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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📑 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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📑 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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📑 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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📑 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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📑 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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📑 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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📑 Job DescriptionJob DescriptionJob DescriptionWe have multiple openings for Life Science Quality Assurance Analysts, Regulatory Affairs Specialist, and Quality Control Analysts. All of these roles will interface with clients on different projects to provide consulting services.We are seeking entry-level experienced personnel or fresh graduate studen ...
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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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📑 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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📑 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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📑 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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📑 By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’s Privacy Notice and Terms of Use. I further attest that all information I submit in my employment application is true to the best of my knowledge. ...
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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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📑 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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📑 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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📑 Takeda Pharmaceuticals Director, PV Risk Management Boston , Massachusetts Apply Now By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’s Privacy Notice and Terms of Use . I further at ...
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📑 By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’s Privacy Notice and Terms of Use. I further attest that all information I submit in my employment application is true to the best of my knowledge. ...
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📑 Director/Assoc Director Regulatory Affairs Associate Director/Director, Regulatory Affairs 2025096 Location: Boston, MA(Remote)Therapeutic Areas: Neuro Job Overview: The Associate Director/Director will develop and implement global regulatory strategies, serving as the regulatory lead for clinical studies and obtaining necessary approvals for ...
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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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📑 Job Description - Clinical Research Coordinator I, Center for Genomic Medicine (3282337) Clinical Research Coordinator I, Center for Genomic Medicine - ( 3282337 ) The Psychiatric and Neurodevelopmental Genetics Unit (PNGU) of the Massachusetts General Hospital (MGH) has an immediate opening for a Clinical Research Coordinator, working u ...
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📑 Job Description - Associate General Counsel & Procurement Director (23000CEC)Job DescriptionAssociate General Counsel & Procurement Director - ( 23000CEC )DescriptionWho We Are:The Executive Office of Energy and Environmental Affairs seeks to protect, preserve, and enhance the Commonwealth’s environmental resources while ensuring and promoting a cl ...
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📑 Associate Director, Regulatory Affairs - Boston, MA - PermanentProclinical is seeking a strategic regulatory leader to join a renowned biotech. This is a permanent position located in Boston, MA.Primary Responsibilities:The primary focus of this role is to work with int ...
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📑 Associate Director, Regulatory Affairs - Boston, MA - PermanentProclinical is seeking a strategic regulatory leader to join a renowned biotech. This is a permanent position located in Boston, MA.Primary Responsibilities:The primary focus of this role is to work with internal and external stakeholders to ensure the timely release of finished product ...
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📑 Associate Director, Regulatory Affairs - Boston, MA - PermanentProclinical is seeking a strategic regulatory leader to join a renowned biotech. This is a permanent position located in Boston, MA.Primary Responsibilities:The primary focus of this role is to work with internal and external stakeholders to ensure the timely release of finished product ...
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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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📑 Were looking for a Medical Director to join a rapidly-expanding Pharma firm based out of Cambridge! In this hybrid role, youll work cross-functionally with key internal players (RWE, HEOR, Medical Excellence, etc.) to design and implement strategies for launch and lifecycle management of pipeline immunology assets, driving innovation to address unm ...
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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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