📑 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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📑 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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📑 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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📑 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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📑 J&J Family of Companies Associate Director, Regulatory Affairs Lincoln , Nebraska Apply Now Associate Director, Regulatory Affairs - 2406166277WDescriptionJanssen Research & Development, LLC, a member of Johnson & Johnson's Family of Companies, is recruiting for an Associate Director, Regulatory Affairs. This position can be located i ...
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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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📑 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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📑 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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📑 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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📑 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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📑 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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📑 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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📑 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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📑 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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📑 Immediate need for Regulatory Affairs Specialist with a Clinical Research Organization in Raleigh. Hybrid position - will work partly in office and partly remote. Looking for a Regulatory Affairs Specialist with at least 2 years of regulatory experience along with submissions. Will work on IND submissions (publishing and structure of the IND, not ...
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📑 Job Title: Regulatory Affairs OfficerCompany: Biopharma OrganizationLocation: Hybrid, RTP AreaBrio Resource Group is a Life Sciences Executive Search Firm committed to providing rare talent on an exclusive search basis to the Biopharma, Pharma, Device and CRO industries. We work on behalf of organizations that value true talent acquisition partners ...
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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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📑 Work at ROCKET PHARMA and help cure rare diseases!Rocket Pharma is a fully integrated, clinical-stage company advancing gene therapies with curative potential for multiple rare childhood diseases. Rocket places enormous value on people and considers team member progress and well-being to be as important as the progress of its pipeline. We are looki ...
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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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📑 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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📑 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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📑 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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📑 At Zimmer Biomet, we believe in pushing the boundaries of innovation and driving our mission forward. As a global medical technology leader for nearly 100 years, a patient's mobility is enhanced by a Zimmer Biomet product or technology every 8 seconds.As a Zimmer Biomet team member, you will share in our commitment to providing mobility and ...
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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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📑 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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📑 Company DescriptionAbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and se ...
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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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📑 **Regulatory Affairs Department Manager, Kfar Saba - OSD, Sterile and Biologics****Location:** Kfar Saba, IL, 1111 ****Company Info****Teva is a global pharmaceutical leader and the world's largest generic medicines producer, committed to improving health and increasing access to quality health solutions worldwide. Our employees are at the core o ...
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📑 Online Application for Assistant Central Intelligence Officer Grade–II/Executive i.e. ACIO-II/Exe in the Intelligence Bureau, (Ministry of Home Affairs), Government of IndiaAbout Assistant Central Intelligence Officer Vacancies in IB:Online applications are invited from Indian nationals for direct recruitment to the post of Assistant Central Intell ...
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📑 Humana Director Public Policy, State Affairs Lincoln , Nebraska Apply Now Become a part of our caring community and help us put health firstThe Director of State Public Policy role resides within the Corporate Affairs Department and will serve as an expert in state public payer, Medicaid and dual eligible public policy while working w ...
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📑 Career CategoryRegulatoryJob DescriptionHOW MIGHT YOU DEFY IMAGINATION?You’ve worked hard to become the professional you are today and are now ready to take the next step in your career. How will you put your skills, experience and passion to work toward your goals? At Amgen, our shared mission—to serve patients—drives all that we do. It is key to ...
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📑 Career CategoryRegulatoryJob DescriptionHOW MIGHT YOU DEFY IMAGINATION?You’ve worked hard to become the professional you are today and are now ready to take the next step in your career. How will you put your skills, experience and passion to work toward your goals? At Amgen, our shared mission—to serve patients—drives all that we do. It is key to ...
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📑 ** Assoc Dir RA, Boston ** Working on rare diseases, obesity, liver in early and mid-phase compounds for a smaller and stable company with higher visibility from an exclusive leadership teamDo you want to be autonomous in your work and interact closely with the leadership team, to have higher visibility and more opportunities to grow …… then this c ...
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📑 US Senior Medical Director, HQ PAXLOVID, Team Lead, MD page is loaded US Senior Medical Director, HQ PAXLOVID, Team Lead, MD Apply locations United States - Pennsylvania - Collegeville United States - New York - New York City United States - Florida - Tampa United States - Massachusetts - Cambridge United States - Connecticut - Grot ...
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📑 Senior Director, Regulatory Affairs (Generalist)Remote Position for West Coast-based candidates, frequent travel to Bay Area requiredMeet is partnering with a late stage pediatric rare disease startup looking for a high-level Regulatory Affairs professional to join their team. This position will be reporting into the SVP of Regulatory Affairs and w ...
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