Manage clinical monitoring activities and overall site management ensuring compliance to the Study Protocol, GoodClinicalPractices (GCPs), ICHguidelines, Federal Regulations, department procedures...
Position Summary: The Senior ClinicalResearchAssociate, reporting to the Director of Clinical Research, is responsible for leading and coordinating activities among participating study physicians...
The CRA II assists in the execution of clinical studies sponsored by Penumbra to assess safety and effectiveness of products. This position works with confidential patient and company data, and...
Description:** The SCRA is primarily a site monitor and is responsible for the management and oversight of their assigned clinical study sites to ensure data quality and patient safety in accordance with ICH-GCP...
Determine if clinicaltrial/study subject documentation aligns with the study hypothesis and monitor clinicaltrial/study safety in accordance with protocols, GoodClinicalPractices (GCP), and regulatory...
South San Francisco, CA (19 miles from Orinda, CA)
45+ days ago
South San Francisco, CA (19 miles from Orinda, CA)
45+ days ago
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...
Position Summary: The ClinicalTrial Associate (CTA) will work with the senior members of the ClinicalTrial Management team to conduct all assigned activities in an efficient and effective manner in...
THE ROLE Reporting to the Senior ClinicalTrial Manager, the Senior ClinicalResearchAssociate will participate in planning and assisting in overseeing the conduct of clinicaltrials in accordance...
, including ICH-GCP and FDA requirements Strong organizational skills and attention to detail, with the ability to manage multiple tasks and prioritize workload effectively Proficiency in using clinical...
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Clinical Research Associate Online Courses and Training Opportunities
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