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IQVIA Holdings Inc
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Mesa, AZ
Maintains current knowledge of local regulatory regulations, and ICH GCP Guidelines for clinical research....
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1 day ago
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Aerotek
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Boston, MA
Job Duties: Regulatory and Study Start-up Subject recruitment, consenting, and screening Subject management Working with the IRB MUST HAVES: MUST HAVE clinical trials experience MUST HAVE regulatory...
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2 days ago
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eclaro international, inc.
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New York, NY
trial conduct, global clinical trial operations, and a thorough understanding of the processes associated with project and study management, knowledge of Good Clinical Practices (GCPs), monitoring,...
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1 day ago
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Ascension Health
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Racine, WI
Coordinates activities for the Institutional Review Board (IRB). Prepares and maintains documents, presentations, files, training materials and databases needed for IRB compliance....
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1 day ago
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Seattle Genetics
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Bothell, WA
The AD ensures that all clinical trials within the program(s) are delivered on-time, on-budget, and with consistency and high quality....
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1 day ago
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Seattle Genetics
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South San Francisco, CA
The AD ensures that all clinical trials within the program(s) are delivered on-time, on-budget, and with consistency and high quality....
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1 day ago
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Idaho Kidney Institute
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Pocatello, ID
One (1) to three (3) years of experience in clinical research required; nephrology experience preferred. Basic knowledge of FDA regulations, IRB requirements and Good Clinical Practice....
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1 day ago
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IQVIA Holdings Inc
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Columbus, OH
Maintains current knowledge of local regulatory regulations, and ICH GCP Guidelines for clinical research....
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1 day ago
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Iqvia
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Augusta, GA
ICH GCP and relevant local laws, regulations and guidelines, towards clinical trial conduct. Broad protocol knowledge. therapeutic knowledge desired....
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1 day ago
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ICON Government and Public Health Solutions
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Gaithersburg, MD
Development of informed consent forms, study documents and study management tools....
Remote Work
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1 day ago
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Fred Hutchinson Cancer Research Center
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Seattle, WA
tasks independently Knowledge of regulations and guidelines for conducting clinical research; for example, good clinical practice (ICH-GCP), Human Subjects Protocol, etc....
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1 day ago
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Aerotek
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Queens Village, NY
PPE provided and COVID screening will take place regularly** Conducts multiple ongoing clinical trials involving patients or healthy volunteers/subjects....
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2 days ago
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Rutgers, The State University of New Jersey
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Newark, NJ
Required Knowledge, Skills, and Abilities Working knowledge of regulatory requirements and Good Clinical Practices ( GCP ) experience....
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2 days ago
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Wills Eye Hospital
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Philadelphia, PA
Applies knowledge of regulatory processes including Institutional Review Board (IRB), Good Clinical Practice (GCP) to all aspects of study conduct Adheres to all hospital, FDA and GCP guidelines Position...
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2 days ago
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Stryker
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Boise, ID
under US Regulations required. + Proficiency in resource planning and clinical trial financial management required. + Must have a demonstrated working knowledge of GCP,, ICH guidelines, and FDA regulations...
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2 days ago
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