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The experienced in-house Clinical Research Associate (CRA) will work closely with the Clinical Operations team in the study set-up, execution, and closeout to ensure study deliverables are met and compliance with clinical protocols, their objectives and ICH and GCP guidelines.
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Clinical Research Associate (CRA): Project related site activities (monitoring, communication) Clinical Project Associate (CPA): Administrative project support. 3 years of experience in clinical research are mandatory, preferably in combination with experience in project management and certain time as field monitor or site coordinator.
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The Associate Director will work closely with HEOR team members and others across the company including market access, marketing, medical affairs, and clinical development to support Insmed's business needs.
$140,000 - $200,000 a yearFull-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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This role will also work closely with global and regional (Osaka, Japan [SHQ]; Florham Park, New Jersey [SI]; and London, England [SEU/SBV]) cross-functional team members including Medical Affairs, HEOR, Clinical Development, Regulatory, Market Access, Commercial teams and external collaborators/vendors to lead and conceptualize research questions, propose study designs, identify appropriate databases, write and review protocols, oversee data analyses, reports, presentations, and publications.
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To drive continued success in this exciting clinical research field, we are seeking committed, skilled, and customer-focused individuals to join our winning team as Associate Director, Statistical Programming for our Bridgewater, New Jersey, USA on-site location, or remotely from a home-based office anywhere in the USA in accordance with our Work from Home policy.
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This position independently manages relationships with internal (CSPV, Regulatory, Clinical, Medical Affairs, HEOR and other stakeholders to ensure expectations are clearly defined and met across participating teams) and external stakeholders.
Full-timeExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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Collaborate with epidemiology colleagues and Product Safety Lead to identify research gaps, develop protocols, conduct analyses, and interpret/communicate scientific findings to internal and/or external stakeholders.
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3+ years of experience in Clinical Research supporting Clinical Trial Managers/Clinical Research Manager on studies. This person will support internally sourced studies and studies out-sourced to Clinical Research Organizations (CROs.
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Profound knowledge of Scientific, Medical, and Clinical Research terminology, such as MedDRA coding. A pharmaceutical company in New Jersey is looking to add a new Senior Pharmacovigilance Associate to their growing team.
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The Associate Director, Clinical Scientist leads in the development, evaluation, planning and execution of hematology oncology clinical studies and ensures scientific integrity and interpretation of study data of a clinical development program.
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Actively contribute to the development of regulatory strategies for investigational products in Investigational New Drug (IND)/ Clinical Trial Applications (CTA), Biologics Licensing Application (BLAs)/ Marketing Authorization Application (MAA), through evaluating scientific merits of Chemistry, Manufacturing and Control (CMC) and nonclinical study data package.
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These business functions include: Clinical Operations, Clinical Development, Biostatistics and Data Management, Regulatory Affairs, Quantitative Clinical Pharmacology, Clinical Safety and Pharmacovigilance, Regulatory/Risk Management, Quality Assurance, Medical Affairs, Translational Research, Research, Informatics Services, Project Management and Operational Management.
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Possesses proficient scientific expertise to propose, design, and execute clinical research and development studies for early and/or late stage assets; able to conceive and communicate strategy proposals well-grounded in supporting literature.
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Occasional travel requiredIQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. Associate, Client Development is responsible for researching competitive information and report enhancements for various parts of the business.
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Basic computer skills to include Word, Excel, as well as proprietary applications unique to the clinical research industry (such as Study Manager) Knowledge base of clinical research with application to multiple Therapeutic Areas.
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clinical research associate jobs in Bernards, NJ
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