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With deep domain expertise in regulatory sciences, clinical research solutions, quality & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma offers an end-to-end suite of fully customizable consulting solutions that de-risk and accelerate our partners’ most high-profile drug and device programs.
Full-timeExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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Minimum 3 years of experience in data programming experience in SAS or R including 2 years in drug development, CRO or other clinical research setting. Minimum 2 years of experience in drug development and/or clinical research.
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The VP, Neuromuscular Clinical Development will partner with AskBio’s Safety and Pharmacovigilance teams to oversee medical monitoring and drug safety reporting, and will work closely with the Clinical Operations, Regulatory, Medical Affairs and Patient Advocacy teams on clinical study planning and resource management to execute global clinical studies.
ExpandApply NowActive JobUpdated 8 days ago - UpvoteDownvoteShare Job
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In short, to be the partner of choice in drug development. As a Site Activation Lead at ICON, you would advance clinical trial start-up activities by understanding the client objectives and assist in the development of the plan for country and site distribution.
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Piper Companies is looking for an experienced Senior Statistical Programmer (PK/PD) to join a well-established, global clinical research organization focused on improving the drug development process and access to therapeutics.
ExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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All applicants must be able to complete pre-employment onboarding requirements (if selected) which may include any/all of the following: criminal/civil background check, drug screen, and motor vehicle records search, in compliance with any applicable laws and regulations.
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10 years in Global or US/EU Regulatory Affairs with 8 years in labeling and/or promotional advertising with excellent knowledge of drug development and regulatory procedures. Lead the implementation of a global labeling development and management strategy, including an thorough understanding of labeling aspects of competitors within relevant therapeutic areas to inform and support competitive labeling.
ExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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We are looking for a talented individual to join our dynamic Drug Product Development team within the Company’s Biologics CMC organization, where we drive the maintenance and evolution of both clinical and commercial products and programs.
RemoteExpandApply NowActive JobUpdated 10 days ago - UpvoteDownvoteShare Job
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Drug, Biologic (IV, Injectable) and Medical Device Development. The Director, Business Development with Cardinal Health Regulatory Sciences is a high-profile position that is focused on new business development (hunting) within biopharma and medical device companies as well as and managing the sales process effectively through to closure and beyond.
ExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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Demonstrated understanding of the overall drug development process with clinical trial design, study implementation, sponsor/site interactions, scientific and clinical methodology, protocol design, project management and regulatory requirements for clinical studies to be reviewed by health authorities.
ExpandApply NowActive JobUpdated 12 days ago - UpvoteDownvoteShare Job
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Professional Knowledge: Thorough understanding of diagnostic technologies, global regulatory frameworks, and biomarker applications in drug development. Extensive oncology experience, including proficiency in target/disease biology, preclinical, and clinical development.
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We are proud to be an EEO employer M/F/D/V. We maintain a drug-free workplace and perform pre-employment substance abuse testing. GM must be able to support the development of a healthy internal culture that retains key employees and encourages their professional development.
ExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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Direct experience with rare disease drug development a plus. Familiarity in the drug development process and prior experience in preparation of original submissions for new drugs preferred.
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The experience of the Verona team, and its highly effective leadership allows us to challenge the status quo in drug development and commercialization. We do this principally through the development of our first-in-class molecule, ensifentrine.
ExpandApply NowActive JobUpdated 16 days ago - UpvoteDownvoteShare Job
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Our client, a major biopharmaceutical company, is seeking a Microbiologist to provide critical support within their Method Transfer and Development Group. This site has flexible, multi-product manufacturing capabilities and facilities focused on testing vaccines intermediates and drug substance, and gene therapy drug substance and drug product.
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drug development jobs in Raleigh, NC
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