Sr Clinical Research Associate jobs at Boston Scientific in United States, Marlborough
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Company (1)
Job type
Job categories
Job title (1)
United States
State
Marlborough
32 jobs found
13.09.2024
BS
Boston Scientific Sr Clinical Research Associate United States, Massachusetts, Marlborough
Source Verification : conducts a comparison of data recorded on Case Report Forms against source documents, verifies Informed Consent Forms for accuracy and completeness, reviews regulatory documents and device accountability...
Bachelor's degree in sciences or healthcare related field, Masters/ PhD is preferred. Minimum 2 years of clinically applied science, or clinical/medical research experience. Demonstrate understanding of medical science and clinical...
Bachelor's degree in sciences or healthcare related field, Masters/ PhD is preferred. Minimum 2 years of clinically applied science, or clinical/medical research experience. Demonstrate understanding of medical science and clinical...
Contributing to protocol, informed consent form (ICF), Investigator’s Brochure (IB), case report form (CRF), and Regulatory submission creation. Executing confidential disclosure agreements (CDAs) and supporting/negotiating creation of clinical study agreements...
Writes study protocols, protocol amendments, informed consents, clinical study project timelines and scientific papers for publication by evaluating scientific literature and publications, analyzing scientific data and staying abreast of current...
Identify scope and comparative information for CES/CRBA, collaborating with cross-functional partners for clinical risk analysis. Conduct literature searches to summarize harms, hazards, alternate therapies, and device-specific benefits; collect primary data...
**This role is open to remote candidates**⦁ Conduct Hands On training in clinical and non clinical settings for physicians and OR Staff in accordance with standardized protocols.⦁ Facilitate didactic sessions...
Source Verification : conducts a comparison of data recorded on Case Report Forms against source documents, verifies Informed Consent Forms for accuracy and completeness, reviews regulatory documents and device accountability...
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