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Deep knowledge of external landscape, drug development, and path to commercialization. 15+ years progressive Biopharmaceuticals experience, with a background in rare disease development. Direct experience in gene therapy and/or gene-editing a plus.
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Knowledge of and broad experience with regulatory procedures and legislation for drug development product registration, line extension and license maintenance in the EU and the US. Our approved treatments are indicated to address high unmet medical needs for serious conditions, and our investigational therapies are in development for patients fighting drug-resistant pathogens.
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Must have a thorough knowledge of clinical research concepts, practices, and FDA regulations and ICH Guidelines regarding drug development phases, clinical trials, clinical study design, and data management methods.
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If you're excited by the challenge of putting protein motion at the heart of drug discovery and passionate about making a difference in the lives of patients, join us! As Vice President of Medical Affairs you will define and implement all aspects of the clinical trial engagement and awareness for Relay Tx's clinical-stage breast cancer program.
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We strive to support and empower every Ironwoodian, providing opportunities to collaborate with colleagues involved in everything we do—from drug development, marketing, technology, legal, specialty sales, and more.
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5+ years of obesity-related clinical development activities with GLP-1 agents and a minimum of 15+ years of relevant drug development experience in the pharmaceutical/biotechnology industry, academic and/or medical research environments, including significant experience leading early and late phase clinical development studies, programs and clinical operations with strong understanding of the elements of drug development programs and experience in their design and execution.
$499,400 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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The Vice President will lead all early development programs from drug candidate selection through to Phase 2 proof of concept. In addition, we are proud of the leading-edge science coming out of our discovery labs, including early-stage research programs that leverage our extensive ion channel expertise and drug discovery capabilities to identify validated drug targets and develop new product candidates.
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Technical Skills: Extensive program management experience in the field of drug development. By focusing on drug repurposing, we aim to provide affordable and accessible therapies for those suffering from diseases that are often overlooked in traditional drug development.
$180,000 a yearFull-timeExpandApply NowActive JobUpdated 20 days ago - UpvoteDownvoteShare Job
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Oversee the development and execution of product intelligence strategies to support the company’s drug discovery and development efforts. Deep understanding of the oncology market, drug development process, and regulatory environment.
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With a combination-focused pipeline that exploits the power of six scientific platforms (Immuno-Oncology, Tumor Drivers and Resistance, DNA Damage Response, Antibody-drug Conjugates, Cell Therapy and Epigenetics) to help address unmet clinical needs in a host of hematological cancers, we are motivated by a dedication to the scientific discovery and collaboration that will one day help eliminate cancer as a cause of death.
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Thorough understanding and working experience of innovative drug development and manufacturing with respect to GMP, quality systems, ICH guidelines, FDA, EMA and associated regulatory requirements.
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Direct the Eurofins Discovery North America Field Sales Team develop best practices for selling to drug discovery researchers and closing business. Expand the Eurofins Discovery market reach by developing strategies to engage Venture Capital Firms, Non-Profit Organizations and Academic Centers.
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The candidate is expected to be influential across the entire drug discovery spectrum in partnership with all research and translational teams, regulatory, toxicology, CMC and clinical. Comprehensive understanding of the entire drug development process, including in-depth knowledge of regulatory environments, clinical development, and Chemistry, Manufacturing, and Controls (CMC.
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In addition, the role will require the development of strong working relationships within Clinical Development Department and with other key functions including, for example, Pharmacovigilance and Drug Safety, Regulatory, Discovery, CMC, Translational, Trial Operations, Biostatistics and Program Management.
$390,300 a yearFull-timeExpandApply NowActive JobUpdated 18 days ago - UpvoteDownvoteShare Job
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Experience in and understanding of end-to-end management of clinical trial conduct, the pharmaceutical industry, clinical drug development, clinical trials operations and regulatory components is essential.
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drug job Title: vice president in Watertown, MA
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