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Requirements: BSc or MSc level degree preferably within the life sciences (PharmD, PhD, or MD preferred) Minimum of 10 years of experience within Regulatory Affairs (Oncology experience preferred) Direct interaction/negotiation skills with regulatory authorities (e.g. FDA, EMA) A broad knowledge of development and life-cycle management is preferred.
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The research portfolio of the Dermatology Service includes optical engineering, artificial intelligence, basic science, translational science, epidemiology and clinical trials with over $5 million of annual funding from NIH, Foundations, Industry, and philanthropic sources.
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Acts as legal advisor for assigned corporate business and functional areas of the Daiichi Sankyo Oncology Business Unit and US Oncology Business Division of the Company (including, for example, Market Access, Sales, Marketing, Medical Affairs) as well as DSI employees performing Global roles in the United States (such as Global Marketing, Global Medical Affairs.
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Possesses the necessary skills to assess scientific merit of all rehabilitation related clinical research proposed to the institution through the use of statistical analyses, research design and methodology and overall clinical value in research in collaboration with the appropriate leadership, principal investigators and grant applications.
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Ashland has an exciting opportunity for a Synthetic Organic/Polymer Chemist to join Ashland Specialty Ingredients G. P. as a member of our Applied Research Team in Global R&D. This position will report to the Applied Research Group Leader in Bridgewater, NJ. This position will be located in Bridgewater, NJ. To learn more about Research & Development at Ashland visit: www.
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On-Board Scientific is hiring an Analytical Research and Development Chemist in New Brunswick/Somerset, NJ! The Analytical Research and Development Chemist will work with an assigned project team of chemists in the laboratory to analyze and develop HPLC and GC methods for assay, impurity and dissolution testing of pharmaceutical finished dosage forms.
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As a Research Scientist, you will work on exciting skin care development. Collects, evaluates and communicates all data collected internally and externally from stability, efficacy and clinical testing and collaborates with Regulatory towards global registration, claims and Quality compliance.
$100 - $114,000Full-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Awesome opportunities to volunteer through Mars Volunteer Program, like volunteering at coral reef cleanups or on research vessels! vet technician (RVT) veterinary technician (LVT) technician specialists (VTS) veterinary technician (CVT.
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They operate a submarine’s sonar, oceanographic equipment, and auxiliary sonar to conduct underwater surveillance, collect scientific data and track enemy targets. Sonar Technician, Submarine (STS) STSs specialize in underwater acoustic technologies.
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Experience and solid knowledge of Pharmacovigilance specificallyProficiency in one or more of these additional areas is a plus: CMC/Mfg., Clinical development and trial execution, Regulatory, Real-World Data and Real-World Evidence, Cell and Gene Therapy, Medical Device, IVD/CDxExperienced in understanding and interpreting regulatory guidelines and documents.
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New Jersey's academic health center, Rutgers Biomedical and Health Sciences (RBHS) takes an integrated approach to educating students, providing clinical care, and conducting research, all with the goal of improving human health.
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The Associate Director, Regulatory Affairs – Regulatory Project Management (RPM) provides planning and drives coordination of global and US regulatory activities. The Associate Director, RPM provides impactful contributions to the RPM group and the regulatory affairs organization by identifying gaps in RPM processes and suggesting and integrating operational and procedural excellence best practice into RPM processes to enhance regulatory affairs capabilities.
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It is preferable that the candidate have experience working in an aseptic manufacturing facility, preferably in quality assurance, manufacturing compliance, clinical quality, or cell therapy. Be responsible for providing quality oversight for site Quality Control laboratories responsible for testing pre-clinical and clinical and commercial stage CAR-T cellular therapy products in accordance with Janssen policies, standards, procedures, and Global cGMP.
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Currently Hiring for Clinical Psychologist, LCSW, LSW, LMSW, LMHC, LMFT,LMHC located in NJ, NY, PA, or MD. Clinical Psychologist (Ph. D, Psy. D, or EdD) Previous clinical experience in Skilled Nursing, Hospital, Hospice, or Home Care setting is a plus.
$110,000 - $145,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Will consider strong Clinical Fellowship Year (CFY) candidate for Long Term Substitute (LTS) positions in the Related Services program. Certificate of Clinical Competence in Speech-Language Pathology (CCC-SLP) is required.
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clinical research scientific affairs jobs Title: director Company: Regeneron Pharmaceuticals Inc in Warren, NJ
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