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Aevi Genomic Medicine
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Wayne, PA
Author key documents needed to conduct clinical trials. Communicates key elements of clinical strategy, issues, and plans to internal and external stakeholders as needed....
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2 days ago
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Editas Medicine, Inc.
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Cambridge, MA
Coordinate Institutional Review Board/Ethics Committee (IRB/EC) approvals, as appropriate....
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1 day ago
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GlaxoSmithKline
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Collegeville, PA
management, global regulatory guidelines and ICH/GCP Experience working with investigators, external experts, Contract Research Organizations and vendors Preferred Qualifications: If you have the following...
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2 days ago
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Escalent
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Livonia, MI
Director, Research & Consulting Life Sciences Sector Our Life Sciences practice works closely with innovative pharmaceutical and biotech companies on some of the most exciting projects in the market...
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13 hours ago
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Emory University
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Atlanta, GA
Associate Director of Research Projects Job Number 50557 Job Type Regular Full-Time Division School Of Public Health Department SPH: Epidemiology This position may involve the following Health and Safety...
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10 hours ago
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JGB BioPharma Consulting
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San Francisco, CA
Requirements: Education: Ph.D. or MD Greater than 2 years experience in pharmaceutical preclinical research Experience working with large animals models in vivo and preclincal large animal study...
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17 hours ago
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GlaxoSmithKline
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Boston, MA
management, global regulatory guidelines and ICH/GCP Experience working with investigators, external experts, Contract Research Organizations and vendors Preferred Qualifications: If you have the following...
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1 day ago
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MacroGenics
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Rockville, MD
Responsibilities and Job Duties Provides input into, and is accountable for Clinical Operations strategy, clinical trial execution, timelines, resource planning, budget forecasting and study management...
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7 hours ago
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University of Colorado
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Denver, CO
trials Competencies: Advanced knowledge of all aspects of clinical trials implementation including Good Clinical Practices, FDA rules and regulations in relation to clinical trials, ICH regulations...
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1 day ago
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Hospital for Special Surgery
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New York City, NY
Clinical Trials Management System implementation and management recommended Thorough understanding of research administration guidelines of Federal and non-Federal sponsors supporting research and educational...
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1 day ago
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ProClinical
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Watertown, MA
Excellent working knowledge of federal regulatory requirements and guidelines for Good Clinical Practice....
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13 hours ago
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Kodiak Sciences Inc
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Palo Alto, CA
trial team and clinical trial sites are properly trained and in compliance with company and/or CRO SOPs, CFR/EMA regulations, ICH GCP guidance, and the study protocol Responsible for oversight of and...
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moments ago
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University of Washington
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Seattle, WA
review board; MINIMUM QUALIFICATIONS Two years of college level course work in a relevant academic area AND two years of experience as a Research Study Assistant OR equivalent education/experience....
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2 hours ago
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Nacho
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Arlington, TX
Support the development and implementation of 2M's clinical research practice with an emphasis on clinical trial monitoring and regulatory affairs, including staff expansion Support the development...
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1 day ago
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Pfizer Inc.
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New Haven, CT
Experience with clinical trial operations Significant track record of experience and accomplishment in clinical and/or research laboratory setting....
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3 hours ago
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