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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 role requires a high-performing and energetic individual who demonstrates outstanding scientific knowledge applicable to hematology or oncology clinical research and the highest personal and ethical standards.
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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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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.
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Understand the impact of DMPK/BA and interdependencies with other functional teams within the enterprise including Pharmacology, Toxicology, Clinical and Regulatory disciplines. Job Description: POSITION Nonclinical Regulatory Document and Scientific Writer.
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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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Eclaro is looking for a Nonclinical Regulatory Document and Scientific Writer for our client in New Brunswick, NJ. Excellent scientific writing, strong QC review skills, and verbal communication skills.
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The successful candidate has a scientific background in operations research, engineering or other STEM field and has expertise in one or more of the following areas: data science, data analytics, data engineering, data visualization, supply chain planning, statistics, machine learning, predictive modeling, decision analysis under uncertainty, artificial intelligence, Python and/or R, app development, and Tableau dashboard development.
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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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The Robert Wood Johnson School of Medicine is consistently ranked as one of the highly NIH-funded academic universities and Rutgers is a member of the Association of American Universities comprising the top research universities in North America.
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Nonclinical Safety (NCS), within Nonclinical Research and Biotherapeutics, is responsible for designing and implementing overall nonclinical safety strategy to support the development and eventual marketing approval and post-marketing safety for the breadth of the BMS portfolio in oncology, hematology, cardiovascular disease, fibrosis, immunology and neurology.
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Primary Talent Partners has a contract opening for a Nonclinical Regulatory Document and Scientific Writer with our client. POSITION Nonclinical Regulatory Document and Scientific Writer.
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CMC regulatory affairs, or a related field within the pharmaceutical or medical device industry. Bachelors Degree (BA/BS) In a relevant field such as Pharmacy, Biomedical Engineering, Chemistry, Biology, or a related scientific discipline is required.
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Must have run and managed RWE and RWD programs in large pharma companies Must have managed a team of 10 people Knowledge of medical affair, scientific affairs and HEOR are preferable Excellent communication and collaboration skills Detailed Job description: Lead the coordination and execution of RWE projects including RWE analytics to address medical gaps within Global Integrated Evidence Generation Plans (IEGPs.
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The RBD role requires a unique set of skills that demands both clinical knowledge, on-label scientific expertise, customer interface team management and leadership skills to provide education and support to providers and patients in the region.
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clinical research scientific affairs jobs Title: director Company: Regeneron Pharmaceuticals Inc in Somerset, NJ
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