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The Cardiovascular & Metabolism Regional Medical Scientific Director is a credentialed (i.e., PhD, PharmD, DNP, MD) therapeutic and disease expert who engages in bidirectional exchange of scientific or medical information with Scientific Leaders (SLs.
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The Field Director is responsible for leading a Oncology Medical Science Liaison (MSL) team in providing scientific, research, and educational support to health care professionals and internal partners related to the current and future Janssen Oncology products.
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The organization has also committed to the development of genetic medicines which includes active investments in Oligonucleotide development, nanomedicines for tissue specific targeting and other gene delivery strategies.
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Reporting to the Associate Director of Engineering, for the Scientific Platforms in the Recursion OS, the Engineering Manager will work to provide first-in-class capabilities and infrastructure that provides robust, configurable, automatable experiment configuration and execution readiness on our Scientific Platforms.
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The Regional Medical Scientific Director (Medical Science Liaison) is a credentialed (i.e., PhD, PharmD, DNP, MD) Director Level Medical Affairs position and therapeutic and disease expert who engages in bidirectional exchange of scientific or medical information with Scientific Leaders (SLs.
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We are seeking a Growth and Improvement minded Regional Medical Scientific Director (AKA Medical Science Liaison / MSL) | in Inflammatory Bowel Disease Immunology that can help drive our Strategic Operating Priorities.
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Consistent adherence to field and corporate policies and Global Medical Scientific Affairs (GMSA) strategy, including field standard operating procedures (SOPs), Good Clinical Practice (GCP) guidelines, and administrative/operational responsibilities.
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Upon Request from Global Center for Scientific Affairs (GCSA) Initiates discussions with SLs and/or potential investigators that include scientific/data exchange within our AOI to determine the alignment with our research strategies, studies concepts, scientific merit, and qualifications for a specific compound or trial.
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Conducts peer-to-peer scientific discussions and maintains a reliable presence with those SLs to ensure they have a medical contact within the company. Develops professional relationships and engages with national and regional SLs to ensure access to company-approved medical and scientific information on areas of therapeutic interest and Company products.
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The Executive Assistant is a key administrative position responsible for supporting and coordinating activities and schedule for the IIRC Scientific Director & Clinical Immunotherapy Director and the Program & Strategy Director.
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The Director collaborates with key stakeholders across the company including Training/Medical Excellence, Field-based/ Medical Outcomes Liaisons (MOLs)/Medical Science Liaison (MSL), market access, payer marketing, global medical strategy, and other HEOR team members, to support Insmeds business needs.
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Maintains a robust Quality Management (QM) program in concert with the Cell Therapies Facility (CTF)Technical Director, Scientific Director and Medical Director. In addition, the QM Director will coordinate quality agreements with internal and external sponsors of cell therapy development and manufacturing for experimental clinical trials.
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Develop and/or maintain an externally funded, independent research/scholarship program, resulting in peer-reviewed publications and other scientific communicationsIn their role as CEDD Co-Director, be an integral member of the CEDD leadership team and work closely with the current co-Director and Director of Education (TBN) in the development of a strategic plan and initiatives to support CEDD’s overall scientific and educational mission.
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The responsibilities of the Laboratory Director shall include professional, scientific, consultative (or advisory), organizational, administrative, and educational matters relevant to the services offered by the Forensic Toxicology Laboratory.
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You will be responsible for providing, scientific leadership, and collaborative working environment to advance the drug candidates from IND through Phase IV. In addition, this position will collaborate with cross-functional stakeholders including in vitro & In vivo pharmacology, clinical biomarkers, DMPK, clinical development and operations, regulatory, CMC, and medical affairs.
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