The Clinical Research Coordinator II (CRC II) will perform research activities using approved techniques, including procuring, processing and shipping research specimens, conducting patient recruitment, and entering data into sponsor-specific electronic data capture forms. The position requires excellent organization and communication skills, as well as the ability to follow-through and prioritize workload.
Requirements
- Evaluate/track the eligibility of all patients seen in the clinic for eligibility in research studies
- Develop and implement patient recruitment strategies
- Conduct telephone interviews and schedules patients for study visits
- Obtain informed consent (for non-treatment studies) and register patients to cohort studies and other protocols
- Review and abstract the medical records for patients, including review of pathology reports
- Enter information into the appropriate EMR and eCRF systems and departmental systems in an accurate manner
- Collect and organize patient data. Review data for quality and completeness and recommends changes to protocols and data evaluation
- Perform clinical tests (Phlebotomy, EKGs)
- Assist with the coordination of the collection, processing, organization, and storage of biological specimens in the systems
- Prepares and presents data reports and findings
- Sends out mailings, takes inventory/ordering supplies, monitoring and set up of equipment
- May be responsible for IRB and regulatory submissions and maintenance of regulatory files
Benefits
- Competitive pay
- Tuition reimbursement and tuition remission programs
- Highly subsidized medical, dental, and vision insurance options
- Career Advancement/Professional Development: Access a wealth of ongoing training and development opportunities
- Pioneering Research: Engage in groundbreaking research projects
