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Oversight and/or contribution to ADME work during drug development may be required. The candidate will conduct in vivo pharmacological experiments using assays relevant to the development of therapeutics for oncology.
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Understanding of scientific principles and regulatory CMC requirements relevant to global drug development and post-market support. Experience providing strategic regulatory guidance to drug development, registration, and post-market support teams.
$165,200 a yearFull-timeExpandUpdated Today - UpvoteDownvoteShare Job
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We are using models early to fail less often, executing clinical trials to add valuation to the company, and generating fit-for-purpose data to feed back into Valos Opal Computational Platform as we reinvent drug discovery and development from the ground up.
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GeneDx is a patient-centric health information company that delivers personalized and actionable health insights that inform diagnosis, guide treatment and improve drug discovery. The National Business Development Director is a field-based sales position responsible for growing revenue and opportunities for GeneDx within the Strategic Accounts and Business Development Enterprise team.
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Stay abreast of the latest fundraising practices and trends in all areas of revenue in general as well as the most up-to-date innovations in renal science, drug development, and the overall pharmaceutical landscape.
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Building upon this track record of establishing a robust pipeline through in-licensing and acquisition of novel assets and technology platforms, Roivant is currently building new capabilities in drug discovery and expanding upon existing development disciplines to become the first large tech-enabled pharmaceutical company.
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Professional Knowledge: Thorough understanding of diagnostic technologies, global regulatory frameworks, and biomarker applications in drug development. Extensive oncology experience, including proficiency in target/disease biology, preclinical, and clinical development.
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8+ years in drug/biologics development in the biotechnology or pharmaceutical industry. This position will lead the implementation of Quality processes and Inspection Readiness Activities, assist with the management of the audit program and partner with key clinical cross-functional groups (e.g., Clinical Operations, Biometrics, Regulatory Affairs) to ensure compliance of Zentalis’ Clinical Development Programs and continuous process improvement.
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A degree in life sciences (or similar field) and advanced Patient Safety and/or Clinical/Drug Development experience. AstraZeneca is a global, science-led, patient-focused biopharmaceutical company that focuses on the discovery, development and commercialisation of prescription medicines for some of the world’s most serious diseases.
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Play a key role in the development of drug-level forecasting for all products in the firm’s portfolio through preparation and review of Wall Street analyst consensus. Work closely with the Treasurer, Accounting VPs, and Senior Finance Associate on modeling updates.
$85,000 - $110,000Full-timeExpandUpdated Today - UpvoteDownvoteShare Job
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Experience in oncology drug development and regulatory sciences with early clinical programs through regulatory interactions, including FIH studies and IND. Keywords : MD, medical doctor, consultant, medical monitor, early clinical development, oncology, cancer, solid tumors, small molecules, targeted therapy, clinical trial, study, protocol, asset, pharma, biotech, biopharma, MD, phase I, first-in-human, FIH, IND, phase II, FDA.
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An understanding of the drug development and commercialization process. Lead the development and evolution of a brand style guide, acts as brand steward. Conceptual leader who sets and consistently rises the bar for content development.
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The Wounded Warrior Project (WWP) Marketing Specialist - Business Development coordinates and executes marketing campaigns and initiatives for WWP peer-to-peer fundraising events driving awareness, acquisition, and fundraising among WWP supporters, donors, and corporate partners.
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Over the past few years, we have been able to significantly expedite the drug development process, evidenced by our acceleration of over 300 clinical trials and reducing trial durations by up to 50.
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Perform clinical duties (e.g. Drug preparation and administration, fibroscan, phlebotomy, ECG, lab processing) within scope. Implement and coordinate assigned clinical trials including start up, vendor management, subject recruitment, source development review, scheduling subjects, protocol training, collection of regulatory documents, conducting visits, ensuring data is entered in a timely manner and all queries are resolved, managing and reporting adverse events, serious adverse events, and deviations, implementing new protocol amendments, providing all close out reports.
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drug development jobs in New York, NY
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