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Our well-proven expertise in medicinal chemistry, customer synthesis, and scale-up process chemistry enables us to support all aspects of drug discovery in a deeply integrated technology-driven platform.
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Minimum of 10 years experience in drug development, clinical research and operational strategy experience including responsibility ensuring studies and programs are executed to quality, timelines and budget (at least part of this time in a Biotech/Pharma environment is preferred.
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Strong demonstration of knowledge of drug development, FDA, EMA and ICH guidelines and regulationsExcellent organizational and communication skills, both written and verbalAbility to work independently as well as part of a team environment.
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Strong understanding of the drug development process including strategic and operational aspects from preclinical through lifecycle management. Director/Senior Director, Program Management Company Overview Repertoire Immune Medicines is a biotechnology company working to unlock and direct the remarkable power of the human immune system to treat cancer, autoimmune disease and infectious disease.
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The CDxL pushes the boundaries of seamless Dx strategy and implementation to select the right patient at the right time, to fulfill regulatory commitment and enable commercial success, thus optimizing access to the right drug, with a patient-centric perspective; Based on this vision, the CDxL is responsible for implementing CDx strategies throughout precision drug development, from early clinical stages to on-market support & life cycle management.
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We are seeking an individual with a technical background, solid working knowledge of GMPs, understanding of the drug development pathway through commercialization, experience interacting with external manufacturers/service providers, and willingness to pivot as priorities change.
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The Director, External Manufacturing, will report to the VP, Commercial Manufacturing & Supply Chain, and is accountable for the business, relationship and operational management of all activities performed within Viridian's Contract Manufacturing Organization (CMO) network (includes biologics Drug Substance and Drug Product manufacturing, device component production, combination device assembly and commercial finished goods production.
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Provides input into the Translational Medicine Plan that defines the biomarker strategy and other aspects to increase the knowledge about the pathway and effects of the drug. The Clinical Research Director (CRD), Amlitelimab, Immunology and Inflammation Therapeutic Area is responsible for the development, execution and reporting of clinical trials in support of the registration of a product, directly reporting to the Clinical Lead in charge of the clinical strategy.
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At 1910 Genetics, we put computation at the heart of drug discovery, blending expertise in computational chemistry, structural biology, pharmacology, genetics, data science, and software engineering to develop drugs for previously undruggable targets.
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In addition, our research team in Vienna, Austria is focusing on new drug discovery and examining the genetic causes of chronic neutropenic disorders. With the April 2024 U.S. approval of our first drug XOLREMDI™ (mavorixafor), we have made great progress in advancing our patient-centric mission and in evolving the company into a fully integrated pharmaceutical company.
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We are pioneers in RNtargeted medicines, and our platform continues to revolutionize drug discovery and transform lives for patients with unmet needs. Associate Director, Commercial Analytics and Operations.
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In this pivotal role, you will provide scientific leadership, people management, and strategic direction, ensuring the delivery of top-quality pathology services for our diverse portfolio of drug discovery and development programs.
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Collaborates with central 340B team to ensure entity compliance with all aspects of the 340B drug discount program. Job Description - Executive Director, Pharmacy-BWH (3304483) Executive Director, Pharmacy-BWH - (3304483.
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Ability to pass a Criminal Offender Record Information (CORI) check, comprehensive background screening, and medical Clinic screening, potentially including a physical examination and drug and alcohol screenings.
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Expertise in one or more technical areas of protein therapeutics development, such as upstream cell culture, downstream purification, analytical, drug product, formulation, or combination product.
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drug job Title: director in Waltham, MA
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