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Medical & Scientific Affairs is responsible for leading evidence generation (including early exploratory pilots phase 3/ 4 clinical trials, external and scientific engagement and internal medical advice on our medicines and the marketplace from a medical perspective.
$297,238 a yearFull-timeExpandApply NowActive JobUpdated 16 days ago - UpvoteDownvoteShare Job
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Understand the impact of DMPK/BA and interdependencies with other functional teams within the enterprise including Pharmacology, Toxicology, Clinical and Regulatory disciplines. Job Description: POSITION Nonclinical Regulatory Document and Scientific Writer.
ExpandApply NowActive JobUpdated 22 days ago - UpvoteDownvoteShare Job
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The Director will develop collaborative partnerships with the cross-functional Insmed team (Medical Affairs, HEOR, Clinical Development, Advocacy, Commercial and Market Access) as well as external medical experts and will have an integral role in driving the planning and execution of scientific communications deliverables across the Insmed respiratory franchise.
$250,800 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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This role is responsible for tactical execution of core medical affairs activities including: HCP and stakeholder interactions (clinical trials, prescribers/providers, KOL development, patient groups, payers), insight capture (advisory boards, real-world data analysis), interpretation of clinical and scientific data, and educational initiatives (medical education, data, value proposition.
Full-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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POSITION Nonclinical Regulatory Document and Scientific Writer. Excellent scientific writing, strong QC review skills, and verbal communication skills required. Partner with Drug Metabolism and Pharmacokinetic (DMPK) and Bioanalytical (BA) Subject Matter Experts (SMEs) to author, review and track regulatory documents.
$60 an hourExpandApply NowActive JobUpdated 20 days ago - UpvoteDownvoteShare Job
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At minimum, a Bachelor’s degree in Chemistry, Biology or related science with a strong background in DMPK and BA including knowledge of the FDA GLPs. Assist with quality review of DMPK reports that are generated by DMPK scientists by fully reviewing the raw data outputs/electronic notebooks and ensuring validity and quality of reported data in the reports, in addition to reviewing DMPK regulatory documents, editing of nonclinical study reports for regulatory acceptance and adherence to company templates, SOPs, DMPK/BA methods, work practices and FDA GLPs, as applicable.
$57 an hourExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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Leads the development of the Global Medical Affairs strategy and execution of the Global Medical Affairs plan for select indications/projects related to evidence generation, medical information and internal education, publications, scientific exchange and external data communication, and stakeholder scientific engagement.
Full-timeExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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Our client, a leading pharmaceutical company, is hiring a Nonclinical Regulatory Document and Scientific Writer, on a contract basis. The post Nonclinical Regulatory Document and Scientific Writer appeared first on TSR Consulting Services.
Full-timeExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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Interface effectively with all other BMS internal stakeholders: Global Medical Affairs functions and other departments, including Commercial, Clinical Research and Development, Regulatory Affairs, Managed Care, Pharmacovigilance, Market Access, Statistics, Translational Research/Development, Project Leadership, etc.
Full-timeExpandApply NowActive JobUpdated 29 days ago - UpvoteDownvoteShare Job
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Create the clinical development strategy for one or more assets in collaboration with the global project team and internal partners such as clinical operations, translational medicine, regulatory affairs, biostatistics, drug discovery, drug safety, marketing.
Full-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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Ensure deliverables are in alignment with business strategy, medical affairs strategy and Insmed clinical development programs. Ability to interpret and organize highly complex scientific data including reviewing pre-clinical and clinical trial data and output from statistical analyses.
$250,800 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Leading pharmaceutical company looking for a Nonclinical Regulatory and Scientific Writer. Job Title : Nonclinical Regulatory Document and Scientific Writer. Leading pharmaceutical company looking for a Nonclinical Regulatory and Scientific Writer.
ExpandApply NowActive JobUpdated 19 days ago - UpvoteDownvoteShare Job
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Through scientific exchange, the MSL will communicate and advance the scientific platform aligned with the overall medical communications and medical affairs strategies. Attend medical/scientific meetings to represent Zealand Medical Affairs with KOLs and other HCPs, strengthen individual expertise as well as capture, integrate, and summarize information of strategic interest.
Full-timeExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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On-Board Scientific is hiring a Nonclinical Regulatory Document and Scientific Writer based out of either New Brunswick, Lawrenceville or Summit, NJ! On-Board Scientific is hiring a Nonclinical Regulatory Document and Scientific Writer based out of either New Brunswick, Lawrenceville or Summit, NJ.
$57.78 - $62.5Full-timeExpandApply NowActive JobUpdated 19 days ago - UpvoteDownvoteShare Job
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You have the power to build, manage, and develop a team of highly competent and engaged managers in the areas of Medical and Scientific Affairs, Medical Information and Pharmacovigilance.
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clinical scientific affairs jobs Company: Regeneron Pharmaceuticals Inc in Bernards, NJ
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