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New York, NY
The position ensures the accurate execution of research protocols in accordance with Good Clinical Practices, HIPAA and required obligations to patient/subject, Principal Investigator, research team...
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3 days ago
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Banner Health
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Phoenix, AZ
Assists in preparing appropriate IRB (Institutional Review Board) forms, informed consents, correspondence with sponsor, etc., in an accurate and timely manner....
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3 days ago
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Mayo Clinic
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Rochester, MN
Review Board (IRB) document preparation and submission; and provides consultative expertise regarding regulatory and policy requirements....
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1 day ago
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University of Florida
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Gainesville, FL
Classification Title: Clinical Research Coord I Job Description: The Department of Medicine, Division of Rheumatology is looking to fill a Clinical Research Coordinator I position....
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1 day ago
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Corcept Therapeutics
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Menlo Park, CA
Responsibilities: Lead multifunctional team through clinical studies activities that meet ICH/GCP and SOP requirements Develop clinical trial protocol synopsis, protocols, amendments and informed consent...
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1 day ago
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Millendo Therapeutics
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Ann Arbor, MI
All work will be completed in compliance with the Standard Operating Procedures (SOPs), Good Clinical Practice (GCP)/International Conference on Harmonisation (ICH) guidelines and other applicable regulations...
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1 day ago
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University of Texas Medical Branch
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Champaign, IL
Clinical Practice (GCP) activities and/or other regulatory activities....
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1 day ago
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Bridgewater, NJ
who has been recognized consistently for the innovative nature of their work, is looking for a Clinical Trial Manager Associate to join their team in Bridgewater, NJ....
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1 day ago
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Senior Clinical Project Manager/associate Clinical Project Management Director, Project Leadershi...
Iqvia
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Washington, DC
Senior Clinical Project Manager/Associate Clinical Project Management Director, Project Leadershi...","datePosted":"2018-10-04","description":" Job Description Join us on our exciting journey!...
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15 hours ago
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Synteract, Inc.
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Carlsbad, CA
The Senior Clinical Project Manager is responsible for the overall coordination and management of clinical trials from start up through close out activities according to contractual time, quality/ cost...
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11 hours ago
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TP Therapeutics
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San Diego, CA
/GCP guidelines, regulatory requirements and clinical trial operations....
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8 hours ago
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Pfizer
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New Haven, CT
The Clinical Project Manager leads the cross-functional execution of one or more clinical studies conducted within the Pfizer Clinical Research Unit (PCRU) and is accountable to PCRU leadership and...
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3 days ago
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Massachusetts General Hospital(MGH)
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Boston, MA
PRINCIPAL DUTIES AND RESPONSIBILITIES : Preparation and modification of Institutional Review Board (IRB) proposals and amendments Maintenance of regulatory binders Direct interaction with study subjects...
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2 days ago
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Madison, NY
Experience in execution of clinical research trials, including GCP and regulatory guideline knowledge and audit inspections....
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2 days ago
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IQVIA
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Cambridge, MA
In depth knowledge of, and skill in applying, applicable clinical research regulatory requirements; i.e., Good Clinical Practice (GCP) and International Conference on Harmonisation (ICH) guidelines...
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1 day ago
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We have received many messages from students asking to make the course more energetic and ... We've listened to you! We fixed all the bugs and added necessary templates and SAMPLE materials. We...
Do you see other people getting their projects done while you struggle with scope creep and are late on deadlines?
Do you want to know how to keep your projects organized and have...
This course is aimed at providing an introduction to project management by PMBOK5 to all risk managers. If you intend to certify or maintain PMI certification you will get, including...
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