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The main function of a clinical research associate is to monitor and oversee clinical trials for new and existing medical products and drugs. They generally work with a sponsor company who has developed some type of medical product and wants to get it approved for sale to the general public. [url=http://www.rtnagel.com/airjordan.php]nike air jordan pas cher[/url] In order to sell this product in doctors offices and pharmacies [url=http://www.1855sacramento.com/moncler.php]moncler outlet[/url] it must be tested extensively and approved for use by the public. Many times clinical research associates work as independent contractors or freelancers. A clinical research associate ensures compliance with clinical trial protocol, and oversees the clinical trial process to ensure it complies with local regulations and general clinical practice. A CRA is usually required to have a degree in Life Sciences and often requires other testing and certifications.

To summarize, a clinical research associate sets up, monitors and completes clinical trials. They are a sort of project manager for medical trials.

But what exactly is a clinical trial and what does it comprise of?

A clinical trial is a type of scientific study that tests the effects, risks, and benefits of a medical product or medication. Several large trials are generally required before a product can be sold to a hospital or local pharmacy. Different types of trials are usually required and include but are not [url=http://www.1855sacramento.com/peuterey.php]peuterey outlet[/url] limited to: trials on healthy patients, trials on sick patients or patients with [url=http://www.achbanker.com/home.php]www.achbanker.com/home.php[/url] a [url=http://s460869484.online.de/index.php?site=forum_topic&topic=39644&page=2]barbour outlet Historytelling[/url] specific condition, and followup trials after the launch of a new product to [url=http://www.mquin.com/giuseppezanotti.php]giuseppe zanotti sneakers[/url] monitor side effects among the general public during mass use.

Some of the typical activities that a clinical research associate may perform on an average day include:

* developing trial protocols
* presenting those trial protocols [url=http://www.vivid-host.com/barbour.htm]www.vivid-host.com/barbour.htm[/url] to a medical committee
* designing data collection forms (case record forms)
* coordinating with ethics committees
* managing regulatory authority applications and approvals
* locating and approving [url=http://www.rtnagel.com/airjordan.php]jordan pas cher[/url] facilities for the trial
* working with doctors and consultants
* prepping the study centers for the trial
* training site staff to industry standards
* monitoring the trial throughout the entire duration
* writing visit reports and documenting the trial
* filing and logging trial documentation and reports
* accounting for unused trial supplies
* archiving study results and documents
* prepping final reports for publication

The job of a clinical research associate greatly varies from one trial to another so take this as a general overview rather than a detailed job specification. With certain companies, the CRA would be involved in [url=http://rover.ebay.com/rover/1/711-53200-19255-0/1?campid=5336182395&customid=pubster&toolid=10013&mpre=http%3A//cgi.ebay.com/ebaymotors/2pcs-Neon-LED-Bike-Car-Tyre-Tire-Green-Valve-Caps-Light-/320518985750]giuseppe zanotti pas cher Get[/url] the entire [url=http://www.1855sacramento.com/woolrich.php]woolrich outlet[/url] trial from start to finish. With others, a medical adviser initiates the trial, and a clinical research associate would then be involved in collecting data and monitoring the trial after it is ready to begin. It is a very important and highly [url=http://www.thehygienerevolution.com/barbour.php]barbour paris[/url] regarded [url=http://www.thehygienerevolution.com/barbour.php]barbour[/url] profession in today s society and will be growing quickly as the population and aging baby boomers continue to expand.

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