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Demonstrated knowledge of principles of drug development, pharmacology, clinical trial methodology and design, medical monitoring of trials, assessment of drug risks and benefits, and safety assessment of drugs both on the market and in development and global safety regulations highly preferred.
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Oversight of the creation of a compelling scientific communications and publication plan based on the clinical trials conducted within Pfizer Oncology. , International Oncology Medical Affairs, Pfizer Research & Development (PRD) cross-TA global Medical platforms, Worldwide Medical, Drug Safety Research and Development and Safety in order to drive TA Medical Strategy across the organization.
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Extensive experience and strong understanding of biopharmaceutical drug development, the competitive landscape / oncology market dynamics / evolving treatment landscape and HCP and patient insights, bringing deep clinical and external stakeholder insights to decision making.
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Oncology medical professional with strong experience (at least 9 years if MD, ClinPharm or MD-PhD, at least 15 years if PhD or PharmD) in the pharmaceutical or biopharma industry with clinical development, and/or medical affairs experience.
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As the medical face of the Pfizer Oncology organization for their portfolio, the incumbent will shape the evidence generation strategies in their portfolio by leveraging their deep expertise that enables the extraction of valuable medical insights from diverse stakeholders in the clinical community.
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The Ivy Research Clinician/Sub-Investigator (Nurse Practitioner) plays an integral role for the safety and well-being of study participants as well as the conduct of the clinical trials.
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Build QSP models integrating biological, pharmacological, and physiological data to support drug development at all stages, from preclinical research to clinical trials and beyond, aiding in dose optimization, biomarker identification, safety and efficacy assessment, drug development decision-making, etc.
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Partner with Clinical Development, Data Sciences, Clinical Trial Supply Management, Drug Safety, Legal, Finance, Product Development, Project Management and Regulatory to ensure operational excellence.
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Represent Pfizer and Pfizer Oncology at the leading Therapeutic Area Medical / Clinical / Scientific Conferences/Congresses, KOL Panels and Clinical Trial Steering Groups, in order to maintain and build relationships with KOLs and the wider clinical community.
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Minimum of 3 years clinical trials experience with a pharmaceutical company, Contract Research Organization (CRO), research center or equivalent required; oncology experience strongly preferred.
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Be a 'voice' for field teams within the Pfizer Oncology organization, ensuring that field medical perspectives are transmitted to discussions of clinical development are integrated into strategy development to support launch and post-launch success.
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Perform regular clinical review of listings and partner with clinical operations/drug safety to develop a safety monitoring plan. 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.
ExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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Several Major Biotech companies are seeking Medical Director/Clinical Scientist with drug development experience to join the Oncology program. Job Duties and Responsibilities are primarily focused, but not restricted to the design, implementation, analysis and interpretation of clinical trials from phase I-III. The candidate will be expected to make a significant contribution to the strategic direction of the Oncology programs, including clinical trial design, implementation, analysis, interpretation and dissemination of results as detailed below.
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Specific areas of work may include clinical trials, patient safety, and global medical affairs. Project Team Involvement: Represent the department on project team(s) to provide functional area input to compound/drug development.
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Medical Directors (Director/SD/ED levels) in Translational Medicine / Clinical Development / Medical Affairs / Drug Safety: 75+ retained assignments. VP, Head of Global Drug Safety & PV | Chinese oncology biotech.
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clinical trials drug safety jobs Title: oncology
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