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QP2-IO team is part of the Global Clinical Development organization and has oversight over drug development aspects related to clinical pharmacology and pharmacometrics of oncology drugs from post-PCC to registration.
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The Oncology Regional Medical Scientific Director, Oncology is a credentialed (i.e., MD, PhD, PharmD, or DNP) therapeutic and disease expert who engages in scientific exchange with leaders in the external medical and scientific community.
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The Director, Health Economics & Outcomes Research (HEOR) Strategy, Oncology leads the strategy development and project execution for on-market and/or pipeline development assets, acting as project decision maker responsible for coordinating the successful development and execution of the HEOR projects for these products.
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The MSL candidate have: Doctorate degree (DVM, MD, PhD, or PharmD) in biological sciences. Experience in Uro-oncology, Urology or Oncology required as a practicing MSL Ability to apply technical expertise and solutions to diverse/individualized situations.
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Registered Nurse (RN), Pharmacist, (PharmD or RPOHs), Medical Doctor (MD) or other clinical experience preferred. The Medical Science Liaison is a United States field-based position and is a key position supporting the Oncology business unit, the sales team and our physician relationships.
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Scientific background in oncology, endocrinology, or neurology is desirable. PhD in a scientific discipline, Medical Degree, or PharmD. As a Regulatory Affairs Sr. Director focused on oncology products, you will lead regulatory strategy, filings, and health authority interactions, providing strategic and operational leadership to support the development of innovative oncology drug products.
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Advanced degree (PharmD, MD, DO, PA, NP, PhD, etc.) Prior drug development experience in oncology is preferred. Title: Contract Director/Sr. Director, Clinical Science (Early Oncology Development.
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The candidate should have an M.D. with board certification/eligibility in hematology/oncology,or a Phd,PharmD with at least 5 years of drug development experience. Provide initial clinical designs for future trials including partnering with research, translational oncology, biostatistics, clinical operations, regulatory and pharmacology for input/alignment and presentation at the Therapeutic Development Team meetings.
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Assists with the recruitment, hiring, and training of pharmacists and technicians for both retail pharmacies and non-retail oncology infusion sties. - Bachelor's degree from an accredited school of pharmacy, Master's degree or PharmD preferred.
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Health sciences advanced or doctoral degrees such as a PharmD, PhD, MD, NP or DMP/ARNP, etc. As part of the Oncology Field Medical team, you will report to Medical Science Liaison Director and work with internal and external partners.
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A high level of emotional intelligence to work effectively with stakeholders. Provide study support from protocol and budget development to submission and completion for Phase IV as well as Investigator Initiated Trials (IITs.
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We are seeking an experienced talented scientist to join the Quantitative Pharmacology and Pharmacometrics – Immune/Oncology (QP2-IO) team in the role of Associate Director QP2-IO team is part of the Global Clinical Development organization and has oversight over drug development aspects related to clinical pharmacology and pharmacometrics of oncology drugs from post-PCC to registration.
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Gilead is hiring an Associate Director level experienced, well-organized professional, who will manage the development of scientific publications and support implementation of the strategic Oncology publication plans for global clinical studies and non-clinical sources, including HEOR, Epidemiology, RWE, Payer, Non-interventional, and database studies, to demonstrate the value of pipeline and inline products in Oncology.
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Masters, with or without PharmD, or equivalent degree with at least six years of experience, where “experience” means having a record of increasing responsibility and independence in a similar role in pharmaceutical drug development.
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Support a high functioning and performance culture for teamQUALIFICATIONS PharmD or PhD requiredExperienced in the diagnosis and treatment of patients with lung cancer within the US Healthcare System8 or more years experience in either pharmaceutical industry, academic centers, clinical practice, or a combination of theseHeadquarters and launch experience strongly preferredKnowledge and experience in lung cancer preferred.
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