The In-House Clinical Research Associate will work closely with the Lead CRA and Investigational Sites by providing support with clinical monitoring activities, assisting with the preparation, organization and follow-up of investigator, site communications and clinical monitoring tracking.
Monitors tracking systems (CTMS, TMF, etc.)
Ability to work well in a team environment but also independently without significant oversight. Flexibility in work hours and readiness to travel.
Medidata RAVE system