Medix

The Clinical research Data Coordinator is a health professional having a working knowledge ofclinical research activities, communication skills and a willingness to cooperate as a team memberand independently accept the challenge of data management specific to a current protocol.. Thisposition will require someone to utilize their clinical knowledge skills to accurately provide data inthe trial EDC system.. Ability to independently exercise judgment, initiative, and resourcefulness in making decisions.. Ability to work cooperatively as a team and with industry professionals.. Knowledge of data management activities as applied to oncology clinical trials.

data manager

The Clinical research Data Coordinator is a health professional having a working knowledge ofclinical research activities, communication skills and a willingness to cooperate as a team memberand independently accept the challenge of data management specific to a current protocol. Thisposition will require someone to utilize their clinical knowledge skills to accurately provide data inthe trial EDC system.Full-time, Monday - Friday, Hybrid or Remote Schedule Flex hoursOvertime permitted with approvalGood Clinical Practice (GCP) certificationBachelor's or equivalent degreeSOCRA or ACRP CertificationsWorking knowledge of Microsoft Word, Excel, OutlookAdvanced Data entry experience in clinical trialsAbility to work effectively under project deadlinesExtensive knowledge of EPIC EMRExtensive knowledge of EDC portals, query resolutionAbility to review and abstract clinical data from electronic and paper source documentsAdvanced-level knowledge of basic anatomy, medical terminology, ability to navigate adverse events, medications, interpret physician's notes, medical records, and laboratory results.Ability to independently exercise judgment, initiative, and resourcefulness in making decisions.Ability to work cooperatively as a team and with industry professionals.Knowledge of data management activities as applied to oncology clinical trials.

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