Wonderful company, great managers.
Pros: global company with a diversified group of people, many clinical trial studies in different indications allowing exposure to many career opportunities
Cons: the databases and systems are very outdated, most are stand alone systems, difficulty in tracking/auditing/quality control measurements
Typical day at work:
-Review clinical documents
-Process FDA requirements
-Track and follow-up missing required documents for ongoing studies
-Prepare contracts and confidential disclosure agreements for new institutions and participating physicians
What I've learned:
-FDA audit preparation activities
-new tracking systems
-supervisory activities
The
– more... hardest part of the job:
-Continuous new system updates
-delay in signatures for contracts, etc.
The most enjoyable part of the job:
-Integral part of clinical trials by ensuring documentation is flawless to help patients receive life-saving drugs
-My co-workers - we are all cross-trained and step up for each other at any time – less