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environment. As a successful candidate, you will: · Manages and maintains protocol documentation and regulatory documents for IRB, DSMB, and PRMC/CPRMC. · Compiles, submits, and processes data
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for the management of the patient. Ensure the consent process is performed in compliance with institutional, FDA, IRB, clinical trial sponsor and other applicable regulations.
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or review informed consent documents · Coordinate responses during the protocol approval process, interfacing with internal stakeholders Your qualifications should include: · Master's degree
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methods and specialized techniques. Keeps abreast of new and improved techniques. Ensures that all laboratory activities are carried out in compliance with each procedure(s) by utilizing safety procedures