📑 University of Oregon Director or Senior Director of Communications, Government and Community Relations Eugene , Oregon Apply Now Director or Senior Director of Communications, Government and Community RelationsApply now ( ...
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📑 University of Oregon Director or Senior Director of Communications, Government and Community Relations Eugene , Oregon Apply Now Director or Senior Director of Communications, Government and Community Relations Apply now ( J ...
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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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📑 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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📑 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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📑 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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📑 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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📑 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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📑 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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📑 Primary Skills:GCP big queryPython programmingStrong SQL Teradata to GCP migrationRequired Skills:· Strong experience in Spark, need to be able to tune the spark jobs.· Strong Python programmer.· Very good experience Bigdata( In GCP it is Data Proc), programming and Had ...
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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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📑 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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📑 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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📑 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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📑 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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📑 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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📑 Primary Skills:GCP big queryPython programmingStrong SQL Teradata to GCP migrationRequired Skills:· Strong experience in Spark, need to be able to tune the spark jobs.· Strong Python programmer.<br ...
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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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📑 I'm partnered with an SF Bay Area-based clinical staged biopharmaceutical company focused on the treatment of liver and cardio-metabolic diseases. This position will be reporting to the VP of CMC and will support the drug development and manufacturing activities for phase 3 and commercialization at CDMOs and CTLs for Biologic programs.Responsibilit ...
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📑 RBW is partnering with an innovative late clinical-stage, oncology Biotech (140 FTE) in their urgent and business-critical search for a new Director/AD, Regulatory Affairs. Our client is focused on discovering and developing precision medicines for the treatment of rare cancer and solid tumours.The candidate will report directly to the Head of RA, ...
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📑 **All applicants must have Project Management experience within the pharma/biotech industry**Summary:We're partnered with a growing gene therapy biotech out of South San Francisco which is looking for a talented Project Manager of R&D to support activities across research, lab operations and Development teams. They are working on a novel non-viral ...
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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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📑 THE COMPANYOur client is a biopharmaceutical company focused on the development and commercialization of innovative therapies for the treatment of liver and cardio-metabolic diseases.THE ROLEWe are looking for a dynamic and experienced AD/Director of CMC Technical Writing with expertise in biologics to join there team. The successful candidate will ...
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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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📑 An exciting biotechnology company are growing out their clinical trial function and consequently, looking for a Director, Clinical Operations to join the team based out of Massachusetts.About the CompanyAt the forefront of groundbreaking clinical trials, this company is spearheading scientific discoveries in the fields of oncology, cardiology, and ...
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📑 Open to candidates from Sr. Clinical Scientist to Director Clinical DevelopmentFully remote arrangement if candidates have Diabetes experience otherwise hybrid is required in Redwood City, CA• Assist with the strategy and creation of the clinical development plans for one or more programs. • Contributed to key strategic documents including clinical ...
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📑 Title: Clinical Trial Patient Safety Specialist Location: Remote | Based in ILPay: $35-47/hr | Based on Location and Experience!Contract: 12+ months SummaryResponsibilities include medical review, which involves in-house review of Case Report Forms (CRFs) including query resolution and addenda writing, QA of data listings.May manage the activities ...
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📑 Requisition Number2229806 Description & Requirements Location: Location: This position can be filled in any of our FORVIS office locations or can be a fully remote work opportunity. Ready to Accelerate Your Career? Join our rapidly expanding advisory team! Our Advisory practice brings our f ...
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📑 Meet has partnered with a notable large pharma that is looking to enhance global well-being by making quality healthcare more affordable and accessible. Their mission unites individuals from diverse backgrounds across nearly 60 countries, all dedicated to improving lives worldwide.The opportunityThey are seeking a dynamic Sr Medical Director/Medica ...
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📑 Overview: HarmonyCares is one of the nations largest home-based primary care practices. HarmonyCares is a family of companies all dedicated to providing high-quality, coordinated health care in the home. This includes HarmonyCares, HarmonyCares Medical Group, HarmonyCares Home Health and HarmonyCares Hospice. Our Mission To bring personalized, qua ...
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📑 Our client is a fast-growing biotechnology company in Los Angeles, CA looking for a Clinical Trial Manager to join their best-in-class Clinical Operations team.This company is working to advance early-phase oncology programs, including a lead ADC program that will soon enter later-phase trials, and anticipates bringing additional compounds into dev ...
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📑 Technical Writer needed for a contract opportunity with Yoh Scientific's client located in Milwaukee, WI area. This position is for a major food manufacturer, and requires experience writing documents describing how to utilize equipment for quality and capacity purposes. Key Responsibilities:Develop comprehensive documentation that meets organiza ...
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📑 Organization & Job SummaryWe are hiring for a QA Director to join a nonclinical CRO working with both small and large animal models while working collaboratively with groups that span biotechnology research. We are in the process of expanding our capabilities by becoming GLP compliant to better serve our sponsor’s needs. We aim to begin generating ...
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📑 Senior Director, Drug ProductDirect Hire Full-Time RoleSalary Range: $224,600 - $245,000 per yearLocation: Redwood City, CA - Hybrid RoleJob Summary:Playing a critical role as the drug product technical lead and CMC project lead, this position will be responsible for drug product development activities leading to NDA submission and commercializatio ...
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📑 Senior Director, Drug ProductDirect Hire Full-Time RoleSalary Range: $224,600 - $245,000 per yearLocation: Redwood City, CA - Hybrid RoleJob Summary:Playing a critical role as the drug product technical lead and CMC project lead, this position will be responsible for drug product development activities leading to NDA submission and commercializatio ...
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📑 Senior Director, CMC Development- APILocation: Charlottesville, VA or Bay Area, CARivus Pharmaceuticals is searching for a Senior Director, CMC Development to set and lead a scalable CMC strategy to advance a new class of investigational medicines called controlled metabolic accelerators (CMAs) that have the potential to improve metabolic health fo ...
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📑 We are searching for a Drug Safety/PV Medical Director MD with 5 years of industry experience to join our biopharma client that has tripled in size over the past few years and is still continuing this impressive growth! This is a great opportunity to join a growing company at an exciting time where you and advance your skills and be a part of their ...
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📑 **Job Description:****Job Summary**The Fulfillment Specialist is responsible for performing tasks involved in processing and shipping orders to the customer for Centralized Services Pharmacy Fulfillment Center.**Job Responsibilities**+ Responsibilities may include: receiving, scanning, picking, packing, auditing and shipping prescri ...
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📑 Beacon Hill Life Sciences is actively recruiting for a Medical Director of Ophthalmology! Location: Fully Remote (EST Hours)Duration: 6-month contract to start with potential to extend based on performance and business needs.Salary Based on experience with approximate rate of $230/hour. To be considered, must have the following: MD with Ophthalmolo ...
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📑 This is a stellar opportunity responsible for leading upstream mammalian cell culture process development and tech transfer activities for the generation of complex molecules including monoclonal antibodies, Antibody Drug Conjugates, Bispecific Antibodies and Fusion Proteins. This is a once-in-a-lifetime Global Expat leadership opportunity within t ...
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📑 Hansoh BioA U.S.-based research & development subsidiary of Hansoh Pharma, Hansoh Bio is a biotech devoted to discovering and developing breakthrough therapies that conquer serious diseases and disorders for patients around the world. Hansoh Pharma is a leading biopharmaceutical company in Asia. Founded in 1995, we are committed to discovering and ...
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📑 This clinical-stage biotech company is revolutionizing the treatment of cancer. They are seeking a Vice President of Regulatory Affairs to oversee all regulatory activities including serving as the primary contact with FDA and other regulatory agencies. You will develop and implement regulatory strategies, lead Health Authority interactions, and ov ...
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📑 THE COMPANY89bio is a clinical-stage biopharmaceutical company focused on the development and commercialization of innovative therapies for the treatment of liver and cardio-metabolic diseases. The company's lead product candidate, pegozafermin (BIO89-100), is a specifically engineered glycoPEGylated analog of FGF21. Pegozafermin is being developed ...
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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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📑 Overview /Benefits Weekend availability preferred, Guard License and Driving License Here at Brosnan Risk Consultants , our culture encourages and supports diversity throughout the workplace! We offer both full-time and part-time opportunities. We also pride ourselves on promoting within. Many ...
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📑 Company Background:Stealth, VC-backed, discovery-stage biotech company with significant funding focused on discovery and development of breakthrough biologics in Oncology and Immunology. This small but experienced team is currently expanding headcount to support the next phase of growth through IND submissions and clinical development.Position Summ ...
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