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Accountable for the scientific guidance and design of the bioanalytical translational and clinical strategies and the execution (e.g. Biomarker) of therapeutic programs with different modalities.
$140,000 - $200,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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7+ years of medical affairs or clinical development background in oncology. Collaborate with medical and clinical operations departments to coordinate the planning, execution, and management of clinical trial activities across medical affairs functions.
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This role will develop and lead all medical affairs activities ensuring partnership within the team (medical strategy, scientific communications and publications) all key Medical Affairs functions (Medical Excellence, HEOR, Field Medical, Medical Information) as well as maintaining a high-level cross-functional collaboration across the organization to ensure alignment and One Insmed approach.
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Closely partner with Research, Clinical teams, Bioanalytics, Regulatory, Project Management, and other R&D functions. The Director of Clinical Pharmacology role within Clinical Development organization will provide leadership and expertise to support assigned clinical pharmacology projects in the clinical development programs for an expanding portfolio of small, biological and inhaled molecules across several disease areas.
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Interact with Regional Market Access/Health Economics / Outcomes Research and Medical Affairs teams to coordinate and develop real world evidence generation in support of their access programs.
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Position Status Full Time Posting Number 24FA0182 Posting Open Date Posting Close Date Qualifications Minimum Education and Experience MD, MD/PhD, PhD, or equivalent terminal degree in cellular, molecular, computational, or systems neuroscience, psychiatry, neurology, or related fields with a research focus on the gut-brain axis.
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Works closely with the Regulatory Affairs labeling group regarding package insert changes to assess and determine the impact of proposed labeling changes on product promotion. Strong business acumen and the ability to see business drivers outside of regulatory affairs.
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Creates demand for BMS medicines by articulating in a balanced manner the clinical and scientific rationale for use of products in appropriate patients. - Excellent communication and presentation skills to articulate scientific and clinical data in an easy-to-understand manner to help HCPs best serve their patients.
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Ability to communicate scientific or clinical data accurately and convincingly to help physicians best serve their patients. - Advanced scientific degree and/or preferred 5+ years of pharmaceutical or biotechnology experience as healthcare sales / MSL / HCP / nurse.
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NJ candidates: hybrid schedule (2x week) Boston candidates: in-person training, fully remote after •Education: minimum qualification is a Bachelors in Biology, or Pharmacy •Must-Have Experience with: VEEVA, life-cycle tools, MS Suite especially Word & Excel •Preferred experience: Regulatory affairs •Work Experience: 5 years of industry experience.
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Prior intern/research lab experience using one of the Machine Learning Engineering / Data Engineering tools – Databricks, Snowflake, Airflow · Extensive Visualization Experience –Tableau/PowerBI work portfolio · Prior intern/research lab experience with ChatBot AI – NLP, Deep Learning, LLM.
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Work At Home Data Entry Research Panelist Jobs - Part Time, Full Time This work-from-home position is ideal for anyone with a diverse professional background, including administrative assistants, data entry clerks and typists, customer service reps or drivers.
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QuidelOrtho unites the strengths of Quidel Corporation and Ortho Clinical Diagnostics, creating a world-leading in vitro diagnostics company with award-winning expertise in immunoassay and molecular testing, clinical chemistry and transfusion medicine.
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On-Board Scientific is hiring an Analytical Research and Development Chemist in New Brunswick/Somerset, NJ! Position Details: Position Type: -year contract with additional opportunity contingent upon performance and continued business needJob Location: New Brunswick/Somerset, NJShift: st shiftCompensation: $ per hour (based on experience) The Analytical Research and Development Chemist will work with an assigned project team of chemists in the laboratory to analyze and develop HPLC and GC methods for assay, impurity and dissolution testing of pharmaceutical finished dosage forms.
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Licensed Clinical Social Worker (LCSW)/ Licensed Marriage and Family Therapist (LMFT) / Licensed Professional Counselor (LPC). We are actively looking to hire talented Licensed Therapists in the Princeton Junction, Brick, Eatontown, Piscataway, North Brunswick, Mt Laurel, Lyndhurst and Cherry Hill, NJ area who are passionate about patient care and committed to clinical excellence.
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clinical research scientific affairs jobs Title: director Company: Regeneron Pharmaceuticals Inc in Raritan, NJ
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