Conducts ECGs and transmits results to clinicaltrial sponsors. Maintains up-to-date and accurate usage logs of samples processed and ECG collections....
Demonstrated knowledge of GoodClinicalPractices and Good Documentation Practices. Demonstrated knowledge of current NIH and/or FDA regulations and guidelines related to clinical research....
Practices (GCPs), ICHGuidelines, AbbVie Standard Operating Procedures (SOPs), and quality standards, ensuring safety and protection of study subjects....
Conducts ECGs and transmits results to clinicaltrial sponsors. Maintains up-to-date and accurate usage logs of samples processed and ECG collections....
Location: Chicago, Illinois Business Unit: Rush Medical Center Hospital: Rush University Medical Center Department: Road Home Research Admin Work Type: Full Time (Total FTE between 0.9 and 1.0)...
What you will be doing: The ClinicalResearchAssociate (CRA) will monitor the progress of clinical studies at investigative sites or remotely, and ensure clinicaltrials are conducted, recorded, and...
Requests new/updated documents from the site/primary assigned CRA, as required Support CRA II, Snr CRA and Lead CRAs in day-to-day studymanagement activities....
Participates in study-related documentation, such as protocol worksheets, procedural manuals, adverse event reports, institutionalreviewboard documents, or progress reports....
Good knowledge of, and skill in applying, applicable clinical research regulatory requirements (i.e., GoodClinicalPractice (GCP) and International Conference on Harmonization (ICH) guidelines)....
Job responsibilities * Performs site qualification, site initiation, interim monitoring, site management and close-out visits (performed on-site or remotely) ensuring regulatory, ICH-GCP and/or Good...
form, and determine if clinicaltrial/study subject documentation is within parameters of study hypothesis, as well as to monitor clinicaltrial/study safety, in keeping with protocols, GCP (GoodClinical...
A CSM is assigned to trial sites to ensure inspection readiness through compliance with the clinicaltrial protocol, company Standard Operating Procedures (SOP), GoodClinicalPractice (GCP), and applicable...
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