CRC I

Job Details:

• Under minimal supervision of the Principal Investigator, assists with administrative activities associated with the conduct of research studies including industry sponsored, grant funded or internally funded studies while maintaining compliance with guidelines set by governing agencies and institutional policy
• Recruit, screen, and enroll eligible study participants
• Manages completion and submission of study related documentation
• Communicates with research sponsor or CRO, local or central IRB, Research and Development, and other ancillary departments to ensure smooth implementation of research protocol and ongoing maintenance
• Assist in monitoring enrollment goals
• Coordinates tasks such as developing informed consents and screening materials, scheduling visits, and acting as a liaison between research participants and the research study team
• Collects data from patient charts, medical records, interviews, questionnaires, diagnostic tests and other sources
• Collect, process, and ship research specimens as directed in the protocol
• Ensure compliance with study protocol and requirements of regulatory agencies
• Tracks and reports adverse events and protocol deviations
• Coordinates all site related monitoring or auditing visits from sponsor or federal agency during the course of the study and at closure
• Under supervision, prepares, submits, and maintains IRB, R&D, FDA and/or any other funding or regulatory documents and research correspondence
• Develops and maintains patient databases and study maintenance logs including but not limited to training logs, delegation of responsibility logs, screening logs, enrollment logs, and investigational product log

Employment Format:

• 2 Month Contract
• Schedule: Monday through Friday 8a-5p
• Pay: $18-20/ hr (any hours over 40 are time and a half pay)
• Working on vaccine trials
• MUST HAVE: previous research experience