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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 21 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 27 days ago - UpvoteDownvoteShare Job
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As part of the Wellness Medical & Scientific Affairs team at Haleon, you will play a pivotal role advancing the trusted science behind our Wellness brands including Centrum, Emergen-C, Benefiber, and Caltrate with new research, claims, and consumer/healthcare professional communications.
Full-timeExpandApply NowActive JobUpdated 19 days ago - UpvoteDownvoteShare Job
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Work closely with individual clinical teams as well as functional area partners (e.g., Translational research, Precision Medicine and diagnostics, Regulatory Affairs, Market Access, Clinical Development) to identify and implement end-to-end Data Science solutions aimed at facilitating decision making.
$244,000 a yearFull-timeExpandApply NowActive JobUpdated 8 days ago - UpvoteDownvoteShare Job
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Accountable for collaboration with cross-functional teams, including research and development, legal, regulatory affairs, and business development, to ensure IP considerations are integrated into product development and commercialization strategies.
Full-timeExpandApply NowActive JobUpdated 27 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.
Full-timeExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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The Scientific Director, US Medical Affairs, Endocrinology will serve as a scientific/medical expert to lead and manage strategic initiatives and projects that integrate Recordati’s scientific, clinical data into programs that drive business and medical affairs priorities.
Full-timeExpandApply NowActive JobUpdated 21 days ago - UpvoteDownvoteShare Job
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Job Title: 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.
Full-timeExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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Good scientific acumen with drug metabolism and pharmacokinetics, and bioanalytical expertise. Excellent communication skills, especially in scientific writing for regulatory authorities.
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The Research Associate II, Formulation Development contributes to the drug discovery and drug product development process by developing and supporting formulations for preclinical and clinical evaluation and performing pre-formulation characterization studies to support drug product formulation development.
Full-timeExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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POSITION Nonclinical Regulatory Document and Scientific Writer. POSITION Nonclinical Regulatory Document and Scientific Writer. Experience reviewing regulatory documents, DMPK and BA reports, and non-GLP/GLP data and notebooks.
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The Scientific Knowledge Engineering team, which sits within the Onyx Product Management organization, is responsible for the data modeling, ontology definition and management, vocabulary mapping, and other key metadata activities that ensure Onyx platforms and data assets speak scientific language.
Full-timeExpandApply NowActive JobUpdated 27 days ago - UpvoteDownvoteShare Job
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The ideal candidate will have a proven track record of conducting clinical research studies, with a focus on conducting oral health clinical trials. The candidate must have 4+ years of clinical research experience (design, implementation, and analysis of randomized controlled trials.
$163,000 a yearFull-timeExpandApply NowActive JobUpdated 27 days ago - UpvoteDownvoteShare Job
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Related fields include Health Services Research/ Outcomes Research/Health Economics, Economics/Econometrics, Pharmacoeconomics, Public Health-Health Policy & Management, Epidemiology, Psychometrics, Statistics/Biostatistics, Pharmacy Administration.
Full-timeExpandApply NowActive JobUpdated 27 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.
$57.8 an hourFull-timeExpandApply NowActive JobUpdated 9 days ago
clinical research scientific affairs jobs Company: Biophase in Piscataway, NJ
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