Protocol Start-Up Coordinator
Location: Richmond, Virginia
Description: VA Commonwealth Univ is currently interviewing Protocol Start-Up Coordinator right now, this job will be presented in Virginia. Further informations about this job opportunity please read the description below. Manages the processes required for identification, assessment, submission and initiation of clinical research trials at the Massey Cancer Center in collaboration with all members ! of the research team. Identifies potential clinical trials to fill out protocol menu. Manages and designs systems to identify, evaluate, and usher new clinical trials through the activation phase. Interfaces with clinical investigators, trial sponsors and others involved in the research process. Develops, establishes and maintains productive relationships with VCU colleagues and customers to achieve essential clinical research outcomes. Meets directly with investigators, regulatory, and administrative supervisors and team members.
Minimum Qualifications
Independent judgment and critical thinking skills. Discretionary decision-making skills. Ability to multi-task and prioritize autonomously. Excellent written & oral communications skills. Ability to work in a fast paced, demanding environment and adapt to changing client status, regulations and work environment. Detail oriented. Significant previous experience in clinical research program management. Experi! ence in an academic medical center preferred. Documented exper! ience interpreting federal, state, and sponsor policies and regulations. Experience with interpreting complex oncology clinical trial protocols and federal, state, local regulations. Knowledge of NCI Cancer Center Support Grant guidelines for clinical research. Experience in the analysis of data and independent generation of customized reports. Ability to work in a demanding, fast paced environment with attention to detail and organization. Highly proficient with multiple computer applications, including but not limited to: Microsoft Word, Microsoft Excel, spreadsheet management, PDF file creation/use, Clinical Trials Management Systems,Internet based research, network & online file maintenance & management, and custom report generation. Demonstrated knowledge of medical terminology. Ability to provide own transportation to attend meetings within the service area or at training locations. BA/BS degree with an emphasis in the basic sciences, healthcare or database design and! management or equivalent training and experience. Certified Clinical Research Professional (CCRP, CCRC, or CCRA) or eligible within one year. Experience using healthcare based clinical information systems preferred. Prior experience working with clinical research sponsors preferred. Experience with Medicare Coverage Analysis decisions preferred.
Preferred Qualifications
Special Requirements
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This job will be opened on: Fri, 10 May 2013 11:30:21 GMT
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