📑 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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📑 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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📑 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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📑 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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📑 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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📑 <p>Roles & Responsibilities :Our Client is seeking a talented Senior Product/ Data Analyst to join our Team. If you are intellectually curious, if you eat/sleep/drink data and are committed to translating data to insights & insights to actionable work items, want new challenges daily, and impac ...
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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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📑 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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📑 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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📑 ** 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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📑 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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📑 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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📑 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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📑 Our client is a leader in developing innovative therapies for a variety of cancers. They are seeking a Director of Oncology Biostatistics to provide scientific and statistical leadership for key molecules. A visible and collaborative role, the Director works in partnership with clinical and regulatory experts to advance the delivery of crucial medi ...
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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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📑 My client, a clinical stage Biopharmaceutical company working on multiple compounds across a range of therapeutic areas, is looking to bring on a Sr Director of Biostatistics. This person will be heading the Biostatistics function! This person will be responsible for the hands on work at a program/study level in addition to leading/managing a small ...
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📑 Our client is an established, mid-sized pharma specializing in developing novel therapeutics in the area of Oncology. They are seeking a Senior Director of Biostatistics to provide statistical input and support for clinical trial design, conduct data analysis, and results interpretation. This role may also be responsible for managing junior biostat ...
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📑 The incumbent will assume a crucial role within the Global Value & Access (GV&A) team, responsible for leading and overseeing statistical activities across a diverse portfolio. This portfolio includes studies related to Alzheimer's disease (AD) dementia and various other projects. In this capacity, you will engage in collaborative efforts withi ...
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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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📑 SummaryOur client, a leading med tech company with over 125 years of experience, has engaged GForce Life Sciences to provide a Sr. Biostatistician. This position will report to the Sr. Director of Biostatistics within the Biostatistics department. This individual will be responsible for collaborating with external partners handling delicate convers ...
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📑 Our client is a biopharmaceutical company with marketed product, a robust pipeline and solid financials, focused in the Rare Disease area. They are currently seeking a Director or Senior Director of Biostatistics (depending on experience) to be responsible for statistical activities supporting clinical trials, including contributing to trial design ...
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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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📑 SummaryIn this position, you will provide overall technical, administrative and functional oversight for the Biostatistics functions of the organization which include statistical consulting, statistical analysis plans, protocols, study reports, and other statistical sections of NDAs and other drug, device, or biologic regulatory submissions. Overse ...
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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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📑 Biostatistician / Senior BiostatisticianW2 Contract to HireSalary Range: $187,200 - $218,400 per yearLocation: Remote Role (PST)Job Summary:We require a biostatistician for systemic amyloidosis studies and to coordinate activities with other functional groups to ensure timely deliverables.Duties and Responsibilities:Provide statistical expertise fo ...
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📑 Biostatistician / Senior BiostatisticianW2 Contract to HireSalary Range: $187,200 - $218,400 per yearLocation: Remote Role (PST)Job Summary:We require a biostatistician for systemic amyloidosis studies and to coordinate activities with other functional groups to ensure timely deliverables.Duties and Responsibilities:Provide statistical expertise fo ...
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📑 RBW has partnered with a patient-focused, mission-driven small biotech in San Francisco in part of their search for a Director of Biostatistics. Reporting to the VP of Biometrics, you will support both early and late phase oncology products, interact with regulatory officials on all statistical related matters, oversee development plans, and provid ...
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📑 Duration: 12 months contract, Full-TimeEmployment Type: W-2Work schedule:• Preferred onsite in Mettawa.• Open to remote for experienced candidates with Medical Claims and EMR experience.Description: The Data Scientist provides analytical support to Scientific Communications and Medical Affairs & HEOR. This position will report to the Director RWE A ...
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📑 About the Opportunity:You will have the opportunity to lead biostatistics activities for innovative clinical trials, contributing to the development of cutting-edge treatments for various diseases. Join our collaborative team of experts to drive statistical strategies and analyses, ensuring the integrity and accuracy of clinical trial data. Work in ...
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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 leveragi ...
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📑 A New Jersey based client asked me to find their next full-time Manager of Demand Forecasting and Analytics. Flexible on-site requirements, looking for ~3 days/week in central New Jersey location.Duties And Responsibilities:Responsible for developing demand forecasts, monitoring forecast performance, maintaining databases related to demand, and per ...
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📑 Summary:The Quality Engineer is responsible for quality control of products, processes, and management systems which includes incoming inspections, product line patrol, outgoing quality control, and updating factory internal quality rules all in accordance with the high industry standards. Responsibilities:Developing and implementing quality stan ...
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📑 Associate Director/Senior Manager, Oncology BiostatisticsLocation: Hybrid SF or PAContact: Susan Devine - sdevine@penfieldsearch.comOur client is a clinical-stage biotech company with an established track record and a strong pipeline in Oncology and Rare Disease, looking for an experienced Biostatistician. This is a hands-on role that will utilize ...
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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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📑 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 dev ...
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📑 Introduction The Department of Corrections is focused on public safety through the custody and supervision of those in our care. Corrections employees have the opportunity to positively impact the lives of others through careers in a variety of fields. Using cutting-edge research and evidence-based approaches, employe ...
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