ClinicalResearchAssociate is responsible for in the execution of clinicaltrials in addition to supporting the study site identification, monitoring plan, and implementation of all aspects of assigned...
Redwood City, CA (10 miles from Moffett Field, CA)
7 days ago
Redwood City, CA (10 miles from Moffett Field, CA)
7 days ago
Position Summary: The Senior ClinicalResearchAssociate (CRA) is responsible for management and monitoring activities that will lead to successful execution of IVD clinical studies....
Piper Companies is currently seeking a motivated ClinicalResearchAssociate with Oncology ClinicalTrials experience to work for a well-established clinical research organization and pharmaceutical...
Computer Skills: Efficient in Microsoft Word, Excel, PowerPoint, Teams and Outlook Familiar with industry CTMS and data management systems Other Qualifications: Understands clinicaltrial processes...
Knowledge, Skills and Abilities: Good knowledge of ICHGCP and FDA/EMA regulations Good verbal and strong written communication skills. Highly organized and detail oriented....
During the close-out visit, the ClinicalResearchAssociate (CRA) must ensure that the clinicaltrial site has complied with the study protocol, GoodClinicalPractice (GCP), and regulatory requirements...
ClinicalResearchAssociate is responsible for in the execution of clinicaltrials in addition to supporting the study site identification, monitoring plan, and implementation of all aspects of assigned...
BeiGene Senior ClinicalResearchAssociate - West Coast in San Mateo , California General Description: The SCRA is primarily a site monitor and is responsible for the management and oversight of their...
to close-out Knowledge of applicable FDA Code of Federal Regulations, GoodClinicalPractices, and ICHguidelines Ability to organize, prioritize tasks, identify and resolve issues efficiently....
Knowledge of applicable FDA Code of Federal Regulations, GoodClinicalPractices, and ICHguidelines Ability to organize, prioritize tasks, identify and resolve issues efficiently....
trials with 3 years as a ClinicalResearchAssociate Strong understanding of GCP, FDA, and ICHguidelines, regulations, and compliance requirements (e.g., 21 CFR 812, ISO14155) Proven ability to manage...
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Clinical Research Associate Online Courses and Training Opportunities
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Everything we do in healthcare has to be discovered and thoroughly tested before it can be put into practice. In this course, you will explore clinical research its challenges and its huge...
Effective data management in clinical trials is the backbone of credible research. Without it, we risk overlooking impactful discoveries and compromising the integrity of groundbreaking...
The Foundations of Clinical Research program is rooted in the belief that clinical research training is critical to professional development in health care. Clinical research training not only...
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