Home Based CRA with True Regional Travel!

Home Based Clinical Research Associate with true Regional Travel!!  Multiple Opportunities!!-Anywhere within 50 miles of an airport!! We are consulting with 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.  Company benefits include: Bi-Annual Merit Increase in Salary, Annual Bonus Averaging 9% of Salary, Excellent Medical Coverage, Home Office Stipend, 401K with Fully Vested Match, Multiple Professional Development Opportunities, Fantastic Training, Home Computer Purchase Assistance, Tuition Reimbursement and On-Going Education! Qualifications & Characteristics Bachelors level degree in a health science or RN A minimum of 1 year field monitoring experience as a CRA Therapeutic Areas: All therapeutic areas of experience will be considered acceptable and reviewed –ability to learn and integrate new/different therapeutic areas Travel requirements: Travel within a 3-5 state region 2-3 days per week, depending on study needs Strong written and verbal communication Outstanding organization skills and attention to detail Strong computer skills: Must have ability to learn new technology and systems Responsibilities:  Position responsibilities will include, but not limited to;· Participate in the identification of potential investigators and clinical sites, conducting pre-study site visits, collecting and reviewing data, and preparing evaluative reports· Conduct clinical site initiation visits, advising and training site personnel on sponsor and regulatory requirements for study conduct and preparing reports· Conduct 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 guidelines· Review 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 required· Provide site support for remote data capture, monitor data capture remotely, review for completeness and consistency, generate and resolve queries between monitoring visits· Assist in the termination of clinical studies through the oversight of clinical sites through data lock, resolving final queries and completing closeout visits We appreciate your understanding, in that; we will only be able to respond to those inquiries who meet the states requirements.  Please include the position ID (CC 517) in the subject line of your correspondence.  Please forward your credentials in Word format, in confidence, to: recruiter7@ccesearch.com .To review additional opportunity statements, please visit our website at: www.ccesearch.com. 630 Davis Drive, Suite 260, Research Triangle Park, NC 27560.  www.ccesearch.com   MRINetwork is the largest and most successful search organization in the world. Each MRINetwork office is a single point of contact to over 1,100 offices in more than 37 countries, our candidates have access to the right jobs virtually anywhere in the world. LOCATION: US-CA-San Diego JOB CATEGORY: Biotech/R&D/Science TYPE: Full Time, Employee JOB REFCODE: CC-517 COMPANY: MRINetwork EMAIL: Apply by Email