We are currently looking to hire Permanent Regional CRAs
The responsibility of a Clinical Research Associate (CRA) is to perform the clinical monitoring aspect of designated projects in accordance with applicable SOP and regulations. Responsibilities include performing clinical on-site monitoring activities (drive patient recruitment, source data verification, drug accountability, data collection), collecting regulatory documentation (when required), performing qualification, ...
We are looking for CRAs with at least 6 years monitoring experience and 3-4 years in Oncology . .
MONITORING – Preparation, conduct, and reporting of selection, initiation/startup, routine/interim and closeout monitoring visits, Site management, Assistance at internal and third-party audits). Assures timely reporting of Adverse Events (AE)/Serious Adverse Events (SAE) and protocol deviations. Maintains regular review of site regulatory binder and ensures proper storage, ...
Our client is currently seeking contract and permanent direct-hire Regional CRAs with a minimum of 2 years of experience in Cardiovascular studies, preferably in Myocardial Infarction and/or device.
Major Roles and Responsibilities:
Demonstrates management of all clinical investigative sites according to the Federal Code of Regulations, Good Clinical Practices, ICH Guidelines, local regulations, and Clinipace SOPs and/or Sponsor SOPs.
Creates quality written trip reports, tracking, and site ...
Serve as the Our Clients subject matter expert on all market research related projects, data and analysis. Initiate and manage all US research activities for Our Clients and obtain, analyze and provide recommendations for market research data of Client’s owners, prospects, competitors, and for various product-related issues in the U.S. market.
1. Initiate and manage all US research activities and programs and identify potential vendors and technologies ...
Mar 18 -
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