Home Based CRA with True Regional Travel

Multiple Opportunities!!-Anywhere within 50 miles of an airport!!

 

We are consulting on behalf of a leading contract research organization, providing a full range of clinical research services for biotech and pharmaceutical clients all over the world. 

 

Opportunity Statement: 

 

The position, created through organic business growth, will work creatively with research sites to facilitate and supervise the conduct of clinical trials, build relationships, and effectively communicate ideas and results throughout a broad spectrum of organizational levels. 

 

Employer Benefits: Bi-annual merit increase in salaryAnnual bonus averaging 8% of salaryExcellent medical coverageHome office stipend401K with fully vested matchMultiple professional development opportunitiesFantastic trainingHome computer purchase assistanceTuition reimbursement On-going education

Qualifications & Characteristics:Bachelors level degree in a health science or RN A minimum of 1 year field monitoring experience as a CRATherapeutic Areas: All therapeutic areas of experience will be considered acceptable and reviewed –ability to learn and integrate new/different therapeutic areasTravel requirements: Travel within a 3-5 state region 2-3 days per week, depending on study needsStrong written and verbal communicationOutstanding organization skills and attention to detailStrong computer skills: Must have ability to learn new technology and systems

Responsibilities:  Participate in the identification of potential investigators and clinical sites, conducting pre-study site visits, collecting and reviewing data, and preparing evaluative reportsConduct clinical site initiation visits, advising and training site personnel on sponsor and regulatory requirements for study conduct and preparing reportsConduct site monitoring visits to identify significant issues and to ensure that all clinical aspects of the studies are being carried out in accordance with GCP/ICH guidelinesReview on-site files and records, case report forms, and source documents for completeness, accuracy, consistency, and compliance; identify deficiencies and discrepancies, provide remedial training and/or initiate corrective action as requiredProvide site support for remote data capture, monitor data capture remotely, review for completeness and consistency, generate and resolve queries between monitoring visitsAssist in the termination of clinical studies through the oversight of clinical sites through data lock, resolving final queries and completing closeout visits

We will only be able to respond to those inquires who meet the stated requirements.  Please include the position ID (CC-517) in the subject lined of your correspondence.  Please forward your credentials in confidence to: recruiter7@ccesearch.com (Word format please).



 

To review additional opportunities, please visit our website at: www.ccesearch.com