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Real Staffing
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Auburndale, MA
Responsibilities: Ensures clinical trials are executed in compliance with ICH/GCP (Good Clinical Practice) guidelines, regulations, and company SOPs Assists in the selection, qualification, and management...
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2 days ago
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Nestle
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Piscataway, NJ
Standard Operating Procedures, applicable laws and ICH Good Clinical Practice....
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3 days ago
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IQVIA
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Morrisville, NC
Working knowledge of current ICH GCP guidelines and applicable regulations. Able to mentor CRAs and more junior Clinical Trial Managers. Able to qualify for a major credit card....
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3 days ago
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Children's Memorial Hospital
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Chicago, IL
Good clinical practices documentation required. 4. Familiarity and experience with FDA and IRB regulatory requirements preferred....
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2 days ago
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Mount Sinai Medical Center
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New York, NY
., Institutional Review Board, Grants and Contracts Office). Duties and Responsibilities: Collects and records study data....
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2 days ago
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Philips
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Maple Grove, MN
Job TitleSenior Clinical Project Manager Job Description In this role, you have the opportunity to The Senior Clinical Project Manager is responsible for managing and meeting the objectives of clinical...
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2 days ago
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University California Irvine
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Placentia, CA
Review Board (IRB), Food and Drug Administration (FDA), and sponsor monitors....
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2 days ago
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IQVIA
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Columbus, OH
Guidelines for clinical research....
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2 days ago
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Massachusetts General Hospital(MGH)
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Boston, MA
GENERAL SUMMARY/ OVERVIEW STATEMENT: The Functional Neurology Research Group (FNRG) is looking to hire a qualified candidate for the position of a Clinical Research Coordinator I position....
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3 days ago
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Celgene Corporation
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San Diego, CA
There are more than 300 clinical trials at major medical centers using compounds from Celgene....
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1 day ago
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IQVIA
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La Jolla, CA
of current ICH GCP guidelines and applicable regulations. + Able to mentor CRAs and more junior Clinical Trial Managers. + Able to qualify for a major credit card. + Valid driver's license; ability...
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2 days ago
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Robsco Search
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Jersey City, NJ
and clinical quality compliance.Strong CRO oversight and operational management skills with proven attention to detail.Advanced knowledge of Good Clinical Practices and current knowledge of FDA regulations...
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2 days ago
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Cincinnati Children's Hospital Medical Center
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Cincinnati, OH
Execute the informed consent process according to Good Clinical Practices (GCP), CCHMC procedures and other applicable policies....
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1 day ago
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Urology San Antonio
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San Antonio, TX
research experience with human subjects Job Type: Full-time Required education: RN or Bachelor's Required experience: Research: 3-5 years...
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1 day ago
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Quadrant Inc
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Bethesda, MD
Clinical Research Coordinator Bethesda, MD MUST: Experienced Clinical Research Coordinator 2+ years clinical research experience Experience with Oncology patients is a must Strong recruitment and retention...
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10 hours ago
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