<http://schema.org/description>
"...Demonstrated successful experience in all relevant clinical data management activities in a BioPharmaceutical or CRO setting* Working knowledge of all phases of clinical trials and ability to assess and determine study requirement from protocol review* Strong Project and Risk Management* CRO and vendor oversight experience preferred* Strong verbal and written communication skills * Consistent, detail oriented, communicative, dedicated to do a job well done* Minimum 5 years Data Management expe..."^^<http://www.w3.org/2001/XMLSchema#string>
<https://tapwage.com/region/4831725-connecticut-usa/sql/jobs>