Clinical Research Associate - General Meds & Oncology
trial reports as assigned Interact with internal work groups to evaluate needs, resources and timelines Act as contact for clinical trial supplies and other suppliers (vendors) as assigned Responsible...
., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines....
Vendor Governance Specialist - Clinical Research
Vendor Governance Specialist - Clinical Research ( at Altasciences in Overland Park, Kansas, United States Job Description Vendor Governance Specialist - Clinical Research (remote) Cypress, CA, USA...
Remote WorkMedical Assistant - Clinical Research, Oncology- Fa
Medical Assistant- Clinical Research, Oncology- Fa at University of Kansas Hospital in Fairway, Kansas, United States Job Description Position Title Medical Assistant- Clinical Research, Oncology- Fairway...
Create Clinical Monitoring Plans (CMP) Performs site qualification, site initiation, interim monitoring, site management and closeout visits (performed on-site or remotely) ensuring regulatory, ICH-GCP...
Research certification preferred such as certified clinical research professional (CCRP) through Society of Clinical Research Associates (SoCRA) or as a certified clinical research coordinator (CCRC...
Clinical Research Associates Oncology Nationwide Pays $60-$80 Per Hour
Earn $60-$80 per hour as a Clinical Research Associate (CRA)- Oncology TotalMed has immediate nationwide contract-to-hire openings for Clinical Research Associates (CRA)- Oncology....
Senior Clinical Research Associate, Internal Medicine, Homeb
Monitors clinical trials in accordance with Good Clinical Practices and procedures set forth by IQVIA Biotech and sponsors....
Senior Clinical Research Associate, Internal Medicine, Homeb
Monitors clinical trials in accordance with Good Clinical Practices and procedures set forth by IQVIA Biotech and sponsors....
Oversee financial aspects of clinical research trial....
Senior Clinical Research Associate I
An equivalent amount of experience can be substituted as appropriate Minimum of at least 2 years of onsite Clinical Monitoring experience Advanced site monitoring; study site management; and registry...
Clinical Research Associate II
An equivalent amount of experience can be substituted as appropriate Minimum of at least 1 year of Onsite Clinical Monitoring experience along with at least 1 year total in clinical research experience...
Senior Clinical Research Associate, Internal Medicine, Homebased, Us - Iqvia Biotechnology
Knowledge of current GCP/ICH guidelines applicable to the conduct of clinical research....
Senior Clinical Research Associate, Internal Medicine, Homebased, Us - Iqvia Biotechnology
Knowledge of current GCP/ICH guidelines applicable to the conduct of clinical research....
Advanced knowledge of applicable clinical research regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines....
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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...
This online course will help you become a more effective clinical supervisor or educator. It is mapped to competences within...
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