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I will be a CRA that is thorough, working to educate staff, monitoring the investigator, and maintaining the data to the best of my ability.
SUMMARY OF QUALIFICATIONS * Broad expertise in data management, drug safety, and clinical operations in different phases of clinical trials within the pharmaceutical industry. Experience in Quality and Risk Management in the medical device industry. * Consistently demonstrate ability to interact positively with senior management with tact and professionalism recognized for dedication and quality of work.
Continued growth, development, and advancement in the field of informatics and/or healthcare related IT
A job! Been laid off since january and would like an in house position with a pharma or device company within a 50 mile radius of 95404
Seeking a contract or full time position that supports inhouse regulatory paperwork and contracts clinical trials in
it should be challenging, involve team work, employee's opinion is heard, performance based reward structure.