📑 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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📑 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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📑 ServiceNow Senior Lead Developer page is loaded ServiceNow Senior Lead Developer Apply locations IND-Hyderabad-Sohini Tech Park, 3rd Floor, Financial District time type Full time posted on Posted Yesterday job requisition id R0027592 It's fun to work at a company where people truly believe in ...
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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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📑 ** 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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📑 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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📑 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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📑 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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📑 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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📑 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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📑 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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📑 Title: Manager/Senior Manager US Regulatory Affairs - Global Development Projects Location: Remote Type: Contract Rate: 52-70 (DOE) Start Date: ASAP Leading Pharmaceutical Company located in NJ is hiring a Manager/Senior Manager US Regulatory Affairs - Global Development Projects with 5+ years industry ex ...
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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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📑 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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📑 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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📑 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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📑 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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📑 locations IND-Hyderabad-Sohini Tech Park, 3rd Floor, Financial District time type Full time posted on Posted 3 Days Ago job requisition id R0027014 It's fun to work at a company where people truly believe in what they are doing! Job Description: Summary:As a Data Security Analyst, you will play a pivotal role in developing ...
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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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📑 locations IND-Hyderabad-Sohini Tech Park, 3rd Floor, Financial District time type Full time posted on Posted 12 Days Ago job requisition id R0027005 It's fun to work at a company where people truly believe in what they are doing! Job Description: Summary:As a Data Security Specialist, you will play a pivotal role in develo ...
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📑 Do you want to be part of a growing world-class organization focused on bettering our world? Are you passionate about significantly improving the future of medicine? Do you believe that people are the most important asset of any company? If so, join AmplifyBio!AmplifyBio is a newly established, commercially focused preclinical CRO that was created ...
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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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📑 Senior Director, CMC Development- Small Molecule TherapeuticsLocation: 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 imp ...
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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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📑 Client Services Project Manager page is loaded Client Services Project Manager Apply locations IND-Hyderabad-Sohini Tech Park, 3rd Floor, Financial District time type Full time posted on Posted Yesterday job requisition id R0027800 It's fun to work at a company where people truly believe in what they are doing ...
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📑 Legend Biotech is seeking Antibody/Protein Discovery Platform Head as part of theResearch & Early Development team based in Nanjing, China.Please note this role is fully based in Nanjing, China and will require onsite presence.Key Responsibilities Develop and lead the Antibody/Protein Discovery Platform and work together within ...
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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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📑 Our passion. Our purpose. At Corbus, it starts at our core.We look for unique talent. Our people are brilliant, they break barriers and are not defined by a title. Eclectic experiences make Corbus a special place to share ideas and grow. At Corbus, transformative ideas can come from anyone, anywhere and anytime. We offer our team flexibility and th ...
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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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📑 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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📑 Senior Director/Director, Global Regulatory AffairsFull-timeOur passion. Our purpose. At Corbus, it starts at our core.We look for unique talent. Our people are brilliant, they break barriers and are not defined by a title. Eclectic experiences make Corbus a special place to share ideas and grow.At Corbus, transformative ideas can come from anyone, ...
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📑 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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📑 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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📑 Pay Range: $118,800.00-$196,200.00 Company Overview: The people of Memorial Sloan Kettering Cancer Center (MSK) are united by a singular mission: ending cancer for life. Our specialized care teams provide personalized, compassionate, expert care to pat ...
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📑 Software Guidance & Assistance, Inc., (SGA), is searching for a Regulatory Affairs Senior Manager for a FULL TIME assignment with one of our premier Pharmaceutical Services clients in Hawthorne, NY.Responsibilities: ...
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📑 Chief Administrative Officer, IND IND (Neurodegenerative Dis) Full Time 77087BR Job Summary The Chief Administrative Officer (CAO) oversees all activities related to the administration of the Institute for Neurodegenerative Diseases (IND), including financial, personnel, systems, program and project, and facilities management. The CAO ensure ...
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📑 Chief Administrative Officer, IND IND (Neurodegenerative Dis) Full Time 77087BR Job Summary The Chief Administrative Officer (CAO) oversees all activities related to the administration of the Institute for Neurodegenerative Diseases (IND), including financial, personnel, systems, program and project, and facilities management. The CAO ensur ...
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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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📑 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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📑 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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📑 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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