The Clinical Research Associate will be responsible for ensuringprotocol procedures are completed accurately, safely, and in a timely manner,this includes responsibility for research assessment and patient interventionunder the supervision of the Principal Investigator. Additionalresponsibilities include regulatory compliance, patient recruitment andenrollment, data collection, research chart documentation, quality assurance,report preparation, protocol information dissemination to health careprofessionals, patients and their family members. You will ensureinvestigational product is adequately managed and documented. Salary range: $24.28-$48.04 Hourly

Required: • Demonstrated clinical research experience, including working knowledge of good clinical practices for clinical research. • Ability to work in more than one environment, travel to participating hospitals, and attend off site staff meetings, conferences and investigator meetings. • Ability to work efficiently and complete tasks with a high degree of accuracy. • Demonstrated organizational skills to handle multiple clinical research projects for efficiency and cost-effectiveness, including handling work delegated by more than one individual. • Excellent English verbal and writing communication skills to convey and obtain information to and from investigators, patients, families, sponsors and co-workers. • Effective interpersonal skills to interact professionally and diplomatically with patients, families, sponsors, co-workers, investigators and others. • Demonstrated skill in prioritizing workflow to meet deadlines, often under pressure of conflicting demands, while maintaining accuracy and effectiveness of work. • Demonstrated computer skills using Word, Excel, email and databases to create reports, correspondence and other documents as required. • Ability to travel between multiple sites to provide coverage and assistance to staff and faculty as required.