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What does clinical trial assistant do?

The CTA is responsible for supporting clinical drug research and development tasks. You work closely with Clinical Research Associates (CRA), who monitor the progress of the study, and Clinical Project Managers (CPM). You may also work with research nurses, researchers and doctors in hospitals.

Who has the responsibility for approving the conduct of a clinical trial?

The individual responsible for the conduct of a clinical study at a site is the principal investigator (PI).

How long does a clinical trial agreement take?

For industry sponsored clinical studies, the clinical contract administrator will review a CTA within two weeks and, following receipt of any responses to queries from the investigator/staff, return the revised draft to the sponsor.

What is a clinical trial agreement?

CTAs are one of several key documents that govern the conduct of clinical trials. A CTA serves as a legally binding contract between a sponsor, site, and researcher, and outlines each partys responsibilities and obligations for the clinical trial.

What is the highline tack trial policy?

ALL SADDLE ORDERS COME WITH A 5 DAY TRIAL PERIOD AND FREE SHIPPING. Simply order the saddle that you are interested in trying through our website by clicking the order for trial button on the saddles page. Full payment will be taken at checkout via credit card, debit card or through our payment plan provider, Affirm

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