Originally Posted by jjjoy
In another thread the topic of jobs in monitoring came up. I've been doing some research into research jobs. I've only heard a little about monitoring. My basic understanding is that this role is review the research site's record-keeping.
Perhaps someone in the know can give me some insight into the pros and cons as well as traits that would be suited to such a position.
I actually don't mind sitting at a computer all day and I can find meticulous record-keeping and reviewing to be satisfying - to a point, of course. I wouldn't say it's fun but I'd MUCH rather do that than run around a hospital floor all day juggling dozens of different priorities. I don't mind working alone for periods, though I dislike working in total isolation. I like having opportunities to meet with others to review our work and to work on improvements. So... does monitoring fit in there?
Depends on the Sponsor, protocol and job description. CRA's usually review medical records, case report forms (data collection tools)regulatory documents, budgets and contracts. You write alot of reports, usually from a template of sorts. You will "track" processes - this means what is done, completed, next steps etc. Computer skills are a must. You will account for investigational products (study drug) or devices. Collaborate with multiple departments - pharmacy/lab/imaging etc. You will ensure regulations are followed - thus you must know them. You will evaluate physicians, nurse and facillities and make recommendations. You will teach - everything from disease process to how to mix a drug. You will often travel all over the country and possibly the world. Can be very rewarding and challenging for the right individual.
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