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📑 The Director Clinical Development will work hand-in-hand with the VP Clinical Development to implement clinical strategies and operationalize in both programs and clinical trials. He/ She will work on the design and execution of clinical trials from early to late stage development through regulatory approval, horizontally leading a matrix team. Thi ...

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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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📑 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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📑 Our client is a commercially successful, oncology-focused biotechnology company that strives to accelerate the discovery, development and commercialization of new medicines for difficult-to-treat cancers.The Senior Medical Director, Pharmacovigilance & Risk Management is responsible for global oversightand management of all medical safety aspec ...

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📑 Career CategorySafetyJob DescriptionHOW MIGHT YOU DEFY IMAGINATION?If you feel like you’re part of something bigger, it’s because you are. At Amgen, our shared mission—to serve patients—drives all that we do. It is key to our becoming one of the world’s leading biotechnology companies. We are global collaborators who achieve together—researching, m ...

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📑 Senior Medical Director, Pharmacovigilance & Drug Safety Boston, MA, USA Req #225 Friday, March 8, 2024 Who We Are: Who We Are: Xenon Pharmaceuticals (NASDAQ:XENE ) is a neuroscience-focused biopharmaceutical company committed to discovering, developing, and commercializing innovative therapeutics to improve the lives of people living ...

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📑 Senior/Executive Medical Director, Pharmacovigilance / Drug SafetyJob Ref : RWIBSMDLocation: RemoteSalary: Competitive Type: Permanent / Full Time RBW Consulting are partnered exclusively with a rapidly growing biotech company based in the New Jersey region. This exciting Oncology organization have had great success already in the clinic, with stro ...

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📑 Associate Director/Director, Pharmacovigilance Scientist Job Ref : RWIBDPVSLocation: RemoteSalary: Competitive Type: Permanent / Full Time RBW Consulting are partnered exclusively with one of the fastest growing biotechnology companies globally. This exciting Oncology organization have had great success already in bringing products to market, with ...

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📑 This role employs entry level programming and design techniques that ensure adherence to software development standards, performance efficiency, reliable and maintainable code, and self-documenting programs. Must have a basic understanding of application development methodologies and techniques. Drafts and updates detailed project plans for small p ...

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📑 About usAlpha-9 Oncology is a clinical-stage biotechnology company developing radiopharmaceuticals for solid and hematologic malignancies. Alpha-9 has a portfolio of molecules entering clinical trials and a robust pipeline of additional targets for future development. With a strong cash position, raised from leading healthcare investors, Alpha-9 is ...

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📑 Vice President, Global Medical Lead About the Company Progressive biotechnology company IndustryBiotechnology TypePublic Company Founded2016 Employees201-500 Categories PharmaceuticalsMedicineManufacturingChemical ProductsConstructionBiotechnology Specialties Protein ...

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📑 Z-Alpha Therapeutics is a pharmaceutical company dedicated to the discovery and development of radiotherapeutics targeting key biological pathways for solid tumors. The company has a revolutionary technology platform in the next generation of alpha particle therapy with potential to be a more targeted therapy, increasing efficacy and limiting toxic ...

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📑 Z-Alpha Therapeutics is a pharmaceutical company dedicated to the discovery and development of radiotherapeutics targeting key biological pathways for solid tumors. The company has a revolutionary technology platform in the next generation of alpha particle therapy with potential to be a more targeted therapy, increasing efficacy and limiting toxic ...

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📑 Job Title: Associate, PV Partner Management Contractor IIOBJECTIVES: The PVAM Specialist will be responsible for supporting the systems, processes and compliance activities for the Global Patient Safety PV Alliance Management function. The PVAM Specialist will provide support to management of pharmacovigilance relevant contracts, Organized Data Col ...

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📑 Job Title: Associate, PV Partner Management Contractor IIOBJECTIVES: The PVAM Specialist will be responsible for supporting the systems, processes and compliance activities for the Global Patient Safety PV Alliance Management function. The PVAM Specialist will provide support to management of pharmacovigilance relevant contracts, Organized Data Col ...

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📑 Senior Business Analyst – Global Patient Safety - PharmacovigilanceDepartment: PharmacovigilanceJob Summary: As a Senior Business Analyst within the Pharmacovigilance group at our client you will play a key role in ensuring the effectiveness and efficiency of our drug safety operations. You will be responsibl ...

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📑 The Executive/Senior Medical Director, Clinical Development will play a vital role in shaping the scientific, clinical, and operational aspects of our client's clinical development programs, focusing on study and program-specific activities. This position will lead the design, planning, and implementation of study protocols for assigned investigati ...

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📑 Executive Director, Drug Safety & Pharmacovigilance About the Company Innovative biopharmaceutical company IndustryPharmaceuticals TypePublic Company Founded2015 Employees51-200 Categories PharmaceuticalsMedicineManufacturingChemical ProductsBiotechnologyHealth CareMedicalTherapeutics ...

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📑 NO C2C, NO 3rd parties, NO relocation candidates consideredSr Director of Medical Safety (Operations)Location: Foster City, CA. (requires on-site time) MUST BE LOCAL CANDIDATES - relocation candidates will not be consideredContract length: 6 months to start - possibility of contract to hire.Compensation:The estimated pay range for this position is ...

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📑 The global safety scientist role is responsible for providing scientific expertise to safety surveillance and risk management activities for MoonLake products in clinical development. The role actively contributes to setting the strategic direction within drug safety and to the development of safety standards and processes.Key Accountabilities:In c ...

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📑 A pharmaceutical company in New Jersey is looking to add a new Senior Pharmacovigilance Associate to their growing team. In this role, the Senior Pharmacovigilance Associate will be responsible for monitoring, processing, controlling, and reporting individual case safety reports and aggregate safety reports for company products.Responsibilities:The ...

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📑 Head, Quality- GCP/GMP/GLP - Small MoleculesLocation: Charlottesville, VA or Bay Area, CA Rivus Pharmaceuticals is searching for a Senior Director, Quality to set and lead a scalable quality strategy to advance a new class of investigational medicines called controlled metabolic accelerators (CMAs) that have the potential to improve metabolic healt ...

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📑 Pharmacovigilance and SafetyProvide services relating to adverse event reporting with a focus on the Final Review step of case processing and any other responsibilities typically associated with, but not limited to, the outlines and responsibilities detailed below.A scalable position requiring 20 - 40 hours per week.This position is Remote/Telecomm ...

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📑 Pharmacovigilance and SafetyProvide services relating to adverse event reporting with a focus on the Final Review step of case processing and any other responsibilities typically associated with, but not limited to, the outlines and responsibilities detailed below.A scalable position requiring 20 - 40 hours pe ...

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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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📑 San Diego-based biotech seeks a Pharmacovigilance (PV) Compliance Manager to ensure the quality and compliance of our pharmacovigilance system. Must be hybrid in San Diego.My client recently received FDA approval for a new product. Key duties include overseeing all DSPV quality and compliance activities, managing deviations, facilitating SOP develo ...

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📑 A pharmaceutical company in New Jersey is looking to add a new Senior Pharmacovigilance Associate to their growing team. In this role, the Senior Pharmacovigilance Associate will be responsible for monitoring, processing, controlling, and reporting individual case safety reports and aggregate safety reports for company products.R ...

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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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📑 The Scientific Team at Russell Tobin & Associates is supporting an exciting pharmaceutical organization that has an opening for an Clinical Quality & Compliance Specialist near San Diego, CA!ResponsibilitiesManage assigned R&D Quality Risk Management activities – assessment of QC of clinical trials execution in a GCP regulated environmentSupport Dr ...

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📑 The Senior Medical Director serves as the Lead Product Safety Physician for multiple or large complex strategically important developmental programs (often multi-indication) and creates and maintains a single interpretation of global safety data for developmental. With the support of Safety Physicians and Safety Scientists identifies and manage ...

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📑 Our client’s vision is to develop curative cell-based immunotherapies for solid tumor cancers. We have innovative science originating from our founder’s world class labs and a unique and disruptive approach to research and development. Our company is first and foremost focused on understanding the science. We are a learning organization, dependent ...

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📑 Our innovative Oncology ADC Pre-IPO biotech client is seeking aMedical Director / Senior Medical Directorwith 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 stageWork ...

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📑 ALSI - Respiratory Medical Affairs Director H/F page is loaded ALSI - Respiratory Medical Affairs Director H/F Apply locations France, Bagneux time type Full time posted on Posted Yesterday job requisition id R10032363 Descriptif de l'entité et de l'activité Avec près de 16 500 collaborateurs, une présence dans ...

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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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📑 NO C2C, NO 3rd parties, NO relocation candidates consideredSr Director of Medical Safety (Operations)Location: Foster City, CA. (requires on-site time) MUST BE LOCAL CANDIDATES - relocation candidates will not be consideredContract le ...

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📑 Job Purpose? The Drug Safety & Pharmacovigilance Physician role is a safety expert medical role contributing to the global safety strategy and overall safety profile for the assigned products throughout lifecycle. Responsibility?Responsible for implementing risk management strategies for assigned product.Lead, set the strategy and when appropriate ...

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📑 Director of Product Compliance Caesars is one of the biggest names in the world of betting and we are striving to become the largest sports betting and iGaming platform in America. We share in our passion to be industry leaders, providing best-in-class service for all our customers. Our Product Technology team has built a prop ...

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📑 Job Purpose? The Drug Safety & Pharmacovigilance Physician role is a safety expert medical role contributing to the global safety strategy and overall safety profile for the assigned products throughout lifecycle. Responsibility?Responsible for implementing risk management strategies for ...

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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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📑 The Senior Director, Drug Safety and Pharmacovigilance is responsible for leading safety surveillance and ensuring compliance with legal and regulatory requirements for pharmacovigilance, signal management, and risk management. - MD degree and board certification preferred - First in Human-Post Marketing experience - 7+ years of experience as a s ...

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📑 Quality Compliance Manager 100% onsite in MA Pay: $60.00 an hour Bachelor's degree with a minimum of 3 years in a quality and compliance role (Pharmacovigilance)Possible contract to hire opportunity DescriptionThe focus for this position is coordinating, managing, and leading a variety of Pharmacovigilance (PV) quality and compliance activities. Th ...

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📑 Beacon Hill Life Sciences is actively recruiting for a Senior Manager of GCP Quality Assurance to work a contract assignment, part-time hours. Part-time, approximately 20 hours per weekDuration of assignment: 6 months with possibility of extensionFully remote is possible, preference though is hybrid (Location: Cambridge, MA)Pay Rate is based on exp ...

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📑 Senior Vice President, Medical, Regulatory & Pharmacovigilance About the Company Pioneering healthcare company IndustryHospital & Health Care TypePrivately Held About the Role The Company is seeking a Senior Vice President for Medical, Regulatory, and Pharmacovigilance. This strategic leadership rol ...

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📑 Our client is a well-established Internet Service Provider (ISP) company offering a range of connectivity solutions spanning from the residential to enterprise levels. They utilize a variety of innovative fiber and splicing technologies to remain on the cutting-edge of their industry. As the company continues to evolve in the rapidly changing ISP i ...

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📑 Director/Sr. Director, Pharmacovigilance, Vaccine SafetyBoston, MAOur client is a clinical-stage biopharmaceutical company focused on developing and commercializing novel vaccines. The ideal candidate for this role will oversee signal and PV life-cycle management and will be involved in a broad variety of PV and clinical safety activities.This is a ...

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📑 Head Global Clinical Franchise RSV Older AdultLOCATIONThe role can be located in Swiftwater, PA or Lyon, France. 2-3 days of on-site presence are required.A world leader in Vaccines, Sanofi has been renewing its pipeline in the area, with the ambition to deliver €10 billion annual sales in the area by 2030, fueled by accelerated innovation. Our gro ...

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📑 Our client, one of the largest independent music festival production companies, is looking for a VP, Creative Production to join their team! The VP, Creative Production is responsible for overseeing the creative production of entertainment, hospitality, leisure, and retail elements of all live events. With a mindset of “experience comes first,” the ...

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📑 The Senior Director, Drug Safety and Pharmacovigilance is responsible for leading safety surveillance and ensuring compliance with legal and regulatory requirements for pharmacovigilance, signal management, and risk management. - MD degree and board certification preferred - First in Human-Post Marketing experience ...

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📑 At Viridian (NASDAQ: VRDN), we aim to advance new treatments for patients underserved by today's therapies. Our team consists of talented, entrepreneurial-minded professionals dedicated to improving the lives of patients suffering from serious diseases. We strive for data-driven decisions, thoughtful risk-taking, and efficient use of time and funds ...

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📑 Quality Compliance Manager 100% onsite in MA Pay: $60.00 an hour Bachelor's degree with a minimum of 3 years in a quality and compliance role (Pharmacovigilance)Possible contract to hire opportunity Description<p ...

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