📑 OverviewJoin a growing Clinical Science team where you will work directly with the VP, Clinical Science. You will support Celldex’s clinical development programs by contributing to the design, data collection, and reporting of clinical studies in a manner consistent with industry standards, applicable regulations and clinical development strate ...
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📑 Reporting to our Senior Director, Drug Product, Process Development, we are seeking an Associate Director to join our team. This position is predominantly a lab-based role and will be responsible for developing scalable processes for LNP delivery of gene-editing RNA cargos. This position will play a critical role in successfully developing manufact ...
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📑 A California-based biopharmaceutical company is looking to add an experienced professional to their CMC Quality Control Department as a Writer / Reviewer. In this role, the CMC Quality Control Writer / Reviewer will be responsible for authoring, drafting. reviewing, and approving the Regulatory QC CMC sections of the company's IND/IMPD and BLA/NDA ...
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📑 RBW is partnered with a large pharmaceutical company that is looking to looking to expand their late phase clinical development team.Job SummaryOur client is looking to hire an experienced Executive Medical Director Clinical Development who is interested in a global development leader / clinical lead role. This person will oversee at least two stud ...
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📑 RBW is partnered with a large pharmaceutical company that is looking to looking to expand their late phase clinical development team.Job SummaryOur client is looking to hire an experienced Executive Medical Director Clinical Development who is interested in a global development leader / clinical lead role. This person will oversee at least two stud ...
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📑 RBW is partnered with a large pharmaceutical company that is looking to looking to expand their late phase clinical development team.Job SummaryOur client is looking to hire an experienced Executive Medical Director Clinical Development who is interested in a global development leader / clinical lead role. This person will oversee at least two stud ...
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📑 GeneCoda has been retained to identify and evaluate candidates for a Chief Medical Officer (CMO) to onboard in late Q2 or early Q3 of 2023 and to be located in the Research Triangle Park, NC. Some relocation assistance can be provided for candidates not already located in the region. Learn why the RTP, NC area as a global life sciences leader m ...
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📑 A clinical-stage biotechnology company based in San Francisco, backed by Third Rock Ventures, is harnessing the power of adipocyte biology and the latest advances in human genetics to develop first-in-class, next-generation medicines for cardiometabolic diseases. The company is building a pipeline of therapies that target rare and common cardiometa ...
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📑 Job Category: Clinical Pharmacology and Drug Development Requisition Number: SENIO001962 Apply now Posted : December 15, 2023 Full-Time Locations Showing 1 location Pudong New District, SH 201210, CHN Description Everest Clinical Research (“Everest”) is a full-service contract research organization (CRO) providing a broad rang ...
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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 is ...
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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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📑 Vice President or Senior Vice President, Regulatory Affairs & Quality AssuranceHybrid Role - San Francisco Bay AreaMeet has engaged on a search for a confidential search for a VP/SVP of Regulatory and Quality with one of our biotech clients. Our client is focused in the Heme/Onc space - you'll be reporting into C-Suite and will be heading up Reg an ...
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📑 The Statistical Analyst will assist asset/study statisticians to fulfill the analytical requests using multiple data sources to answer questions related to clinical trials and epidemiological research on vaccine development in pharmaceutical settings. The analyst will use statistical software to analyze, summarize and report data. This person will ...
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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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📑 Clinical Development Leader (Medical Director to Senior Director level)San Francisco (remote/hybrid) **MUST reside on the West Coast or willing to relocate**Full-timeSciPro is working with one of the most exciting names in Oncology. This position holds high visability and will report directly to the CMO.My client is on the verge of going public due ...
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📑 Clinical Development Leader (Medical Director to Senior Director level)San Francisco (remote/hybrid) **MUST reside on the West Coast or willing to relocate**Full-timeSciPro is working with one of the most exciting names in Oncology. This position holds high visability and will report directly to the CMO.My client is on the verge of going public due ...
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📑 Study Responsible PhysicianOngoing ContractPart Time Hours: 10-20 hours a week RemoteEducation and Experience:University degree - MDPreferably experience in drug/clinical development and/or registry, surveillance studies (e.g. Project Management, Pharmacovigilance, Medical Affairs, RWE, Clinical Pharmacology, study operations)Post-marketing surveil ...
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📑 Introduction This examination is being given to fill one vacancy in the Emergency Medical Services Department and to establish an eligible list to fill future vacancies. Resumes will not be accepted in lieu of an application. A completed application must be postmarked or received online by the final filing deadline. < ...
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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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📑 Director, CMC Regulatory AffairsDirect Hire Fulltime RoleSalary Range: $208,000 - $235,000 per yearLocation: Redwood City, CA - Hybrid RoleJob Summary:The position is responsible for providing CMC regulatory strategies and leading the preparation of CMC sections of regulatory submissions to support the clinical development and eventual marketing ap ...
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📑 Director, CMC Regulatory AffairsDirect Hire Fulltime RoleSalary Range: $208,000 - $235,000 per yearLocation: Redwood City, CA - Hybrid RoleJob Summary:The position is responsible for providing CMC regulatory strategies and leading the preparation of CMC sections of regulatory submissions to support the clinical development and eventual marketing ap ...
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📑 Senior Problem Analyst/ Senior Problem Manager page is loaded Senior Problem Analyst/ Senior Problem Manager Apply locations IND-BLR-Divyasree Technopolis time type Full time posted on Posted Yesterday job requisition id R0086994 Responsibilities:• Perform root cause analysis (RCA) for cases in scope, and for mor ...
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📑 This is an opportunity to work with an innovative biotechnology company working on the development and manufacturing of small molecules for a diverse portfolio of therapeutic targets. To support the continued growth of the pipeline, we are looking for an experienced Senior/Executive Director of CMC to guide strategy.Responsibilities:Oversee vendors ...
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📑 This is an opportunity to work with an innovative biotechnology company working on the development and manufacturing of small molecules for a diverse portfolio of therapeutic targets. To support the continued growth of the pipeline, we are looking for an experienced Senior/Executive Director of CMC to guide strategy.Responsibilities:Oversee vendors ...
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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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📑 Director, Clinical Development - Immunology*Remote for East Coast Candidates*Meet has partnered with a well-established pharma based on the East Coast! They are looking for a Director of Clinical Development to join their immunology department. This position will be reporting into a Senior MD and will be supporting multiple global clinical programs ...
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📑 We are seeking a highly motivated and enthusiastic lead in upstream process development located in Mount Prospect, IL. The successful candidate will be supervising a team that develops and implements mammalian cell culture processes for the production of biological therapeutic proteins. You and your team will be responsible for the scale-up, proces ...
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📑 About Firefly Bio:Firefly specializes in Degrader Antibody Conjugates (DACs) which combine the unique strengths of ADCs with selective protein degraders. Our state-of-the-art platform results in highly specific delivery of degraders to target tissue. Our mission is to realize the full potential of ADCs by unlocking new classes of payloads. Our comp ...
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📑 About Firefly Bio:Firefly specializes in Degrader Antibody Conjugates (DACs) which combine the unique strengths of ADCs with selective protein degraders. Our state-of-the-art platform results in highly specific delivery of degraders to target tissue. Our mission is to realize the full potential of ADCs by unlocking new classes of payloads. Our comp ...
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📑 RBW is partnering with an innovative clinical-stage, Biotech in their search for a newly created position - (Sr.) Director, R&D Quality Assurance. Our client is focused on discovering and developing medicines for the treatment of Crohn's and other inflammatory diseases.The candidate will report directly to the Head of QA, and this role will be resp ...
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📑 Our innovative Oncology ADC Pre-IPO biotech client is seeking a Medical Director / Senior Medical Director with strong Oncology Clinical Development experience to cover development programs spanning phases I, II, III.Responsibilities:Providing clinical leadership; from early-stage clinical trial design for novel cancer drugs through to CoP stageWor ...
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📑 About LexeoLexeo Therapeutics is a New York City-based, clinical-stage genetic medicine company dedicated to transforming healthcare by applying pioneering science to fundamentally change how genetically defined cardiovascular diseases and APOE4-associated Alzheimer’s disease are treated. Using a stepwise development approach, Lexeo is leveraging e ...
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📑 About Firefly Biologics:Firefly Biologics is a Bay Area venture-backed company currently operating in stealth mode. Our mission is to unlock the full potential of bioconjugates and develop medicines with long-lasting benefits for patients. We are establishing an expert team to build state-of-the-art platform capabilities for the invention and devel ...
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📑 A clinical-stage biotech focused on Rare Diseases. This company utilizes antibodies to harness the bodies immune system to fight off disease.The RoleThis person ill serve as the GRL for the company's early stage proprietary pipeline as well as supporting partnered programs with large pharma , reporting into the SVP of Regulatory Affairs.Main Respon ...
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📑 RBW is partnering with an innovative clinical-stage, Biotech in their search for a newly created position - (Sr.) Director, R&D Quality Assurance. Our client is focused on discovering and developing medicines for the treatment of Crohn's and other inflammatory diseases.The candidate will report directly to the Head of QA, and this role will be resp ...
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📑 ** Principal / Associate Director, Statistical Programmer - Biotech - California **Partnered with an exciting Biotech seeking a Principal / Associate Director, Statistical Programmer to join their team.This company is in a very exciting unmet need and could be the first approved treatment in this area.Chance to work with a proven leader and be part ...
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📑 ** Principal / Associate Director, Statistical Programmer - Biotech - California **Partnered with an exciting Biotech seeking a Principal / Associate Director, Statistical Programmer to join their team.This company is in a very exciting unmet need and could be the first approved treatment in this area.Chance to work with a proven leader and be part ...
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📑 Duties And Responsibilities:Responsible for developing demand forecasts, monitoring forecast performance, maintaining databases related to demand, and performing statistical and other quantitative analyses to ensure accurate and effective demand forecasting. You will analyze large datasets and perform quantitative analysis to identify industry tren ...
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📑 Job Title - Statistical Science Associate DirectorAbout AstraZenecaAstraZeneca is a global, science-led, patient-focused biopharmaceutical company that focuses on the discovery, development and commercialisation of prescription medicines for some of the world’s most serious disease. But we’re more than one of the world’s leading pharmaceutical comp ...
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📑 Duties And Responsibilities:Responsible for developing demand forecasts, monitoring forecast performance, maintaining databases related to demand, and performing statistical and other quantitative analyses to ensure accurate and effective demand forecasting. You will analyze large datasets and perform quantitative analysis to identify industry tren ...
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📑 The Senior Manager provides timely support to the team on all programming matters according to the project strategies within a therapeutic area. As a part of a project team, the incumbent provides project leadership and contributes to the programming support for processing data from clinical studies. Project requirements will be identified accordin ...
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📑 Mantell Associates is partnered with an organisation searching for a highly skilled and experienced Principal Statistical Programmer to join their biometrics division.Principal Statistical Programmer - Responsibilities:Play a pivotal role in leading statistical programming activities for multiple clinical trials, ensuring the timely and accurate de ...
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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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📑 At Eisai, satisfying unmet medical needs and increasing the benefits healthcare provides to patients, their families, and caregivers is Eisai's human health care (hhc) mission. We're a growing pharmaceutical company that is breaking through in neurology and oncology, with a strong emphasis on research and development. Our history includes the devel ...
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📑 Title: Director/Senior Director of Regulatory Salary: $200,000 to $270,000Summary: An Oncology based biotech client of ours is looking to fill their Director/Senior Director role based out of their facility in the San Francisco Bay Area. They are looking for very committed and passionate candidates who can collaborate with their colleagues to help ...
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📑 Title: Director/Senior Director of Regulatory Salary: $200,000 to $270,000Summary: An Oncology based biotech client of ours is looking to fill their Director/Senior Director role based out of their facility in the San Francisco Bay Area. They are looking for very committed and passionate candidates who can collaborate with their colleagues to help ...
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📑 Fantastic new opportunity for an experienced toxicologist at a brilliant biotech company!My client is looking for a highly knowledgeable, competent and detail-oriented Toxicology Consultant with extensive responsibility for designing, monitoring and reporting results of in vitro and in vivo preclinical pharmacology and toxicology studies. Experienc ...
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📑 About Stripe Stripe is a financial infrastructure platform for businesses. Millions of companies—from the world’s largest enterprises to the most ambitious startups—use Stripe to accept payments, grow their revenue, and accelerate new business opportunities. Our mission is to increase the GDP of the internet, and we ha ...
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📑 Job Title: Head of Biology & Translational ScienceLocation: San DiegoBackgroundRayzeBio is a dynamic biotechnology company headquartered in San Diego, CA. Launched in late 2020 and recently acquired by Bristol Myers Squibb (BMS) as a wholly owned subsidiary, the company is focused on improving survival of people with cancer by harnessing the power ...
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📑 Munkebo Seafood tilbyder et job i en mindre produktionsvirksomhed, hvor den rette person vil få stor indflydelse på opgaverne indenfor sit ansvarsområde og få mulighed for at præge beslutningerne og fremtiden. Hos Munkebo Seafood A/S er der ikke langt til beslutningerne, og de deltager alle aktivt i hverdagens udfordringer og hjælper hinanden, hvis ...
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