Our client is looking for a Meditech Analyst for a Consult-to-Hire opportunity.
Seeking someone with 3-5 years of EMR experience, preferably Meditech
(client is also using Greenway and eClinicalWorks).
*Experience with building and maintaining modules
MODULES IN ORDER OF IMPORTANCE
*Training IMO - Intelligent Medical Objects (IMO®)
*Discharge Routine - in-patient modules
*ER Module (EDM)
*Meaningful Use – Stage 1 pulling data (Stage 2 experience would be a plus but not required)
File complex regulatory documents
Coordinate scanning of all related clinical trial documents
Ensure that all clinical trial documents are prepared accurately
Interact with trial personnel to ascertain any needed detail for documentation
Prepare all trial documents for inspection
Ensure that the appropriate data dictionaries are updated for new clinical trials
Must have ICH and FDA GCP
Knowledge of country specific regulatory regulations
Understanding of regulatory ...
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