Clinical Research Coordinator

Job Duties

• Interacts with co-workers, visitors, and other staff consistent with the values of Jefferson.
• Performs a variety of research, data base, biospecimen collection and processing, as well as clerical duties in support of clinical trials to assist investigators in organizing, gathering and compiling clinical research data.
• Organizes and maintains documentation required for clinical trial(s).
• Informs Principal Investigator and/or designated individual on any issues concerning patients response to treatment/medication/any adverse effects overall to patients.
• Aids in regulatory body filings including IRB submissions.
• Might assist in the enrollment of human subjects.
• Might provide clerical and technical support to ensure adherence to research protocols and quality of information received.

Minimum Qualifications

• High School Diploma/GED or equivalent.
• 4 years of relevant experience.
• Knowledge of and the ability to utilize technology tools to organize, store and manage database systems.
• Knowledge of and ability to utilize tools, techniques and processes for gathering and reporting data in a particular department or division of a company.
• Knowledge and understanding of legislation and regulatory bodies affecting healthcare practices.
• Ability to manage multiple concurrent objectives, projects, groups, or activities, making effective judgments as to prioritizing and time allocation.

Physical Demands

• Lift and carry 40-50 lbs.
• Frequent to continuous standing/walking.
• Patient transporters can walk 8-10 miles per shift.
• May kneel, bend, squat and perform CPR.