Clinical Research Coordinator
About The Position
Under general supervision of the Director, the Clinical Research Coordinator provides support for multi-center, multi-year studies at the Emergency Medicine Network (EMNet) Coordinating Center (www.emnet-usa.org). The major research activities at this time involve (a) prospective cohort studies; (b) the National ED Inventories (NEDI), which includes a database of every ED in the United States; and (c) studies on prehospital and emergency department systems of care, such as for maternal health and respiratory emergencies. EMNet's mission is to advance public health objectives through multicenter, emergency department-based research. EMNet involves >200 medical centers. Following established policies, procedures, and study protocols, provides assistance on clinical research studies, including recruiting, evaluating, and consenting patients for studies; collecting and organizing patient data; scheduling patients for study visits; performing clinical tests such as phlebotomy, EKGs, etc.; and maintaining and updating data generated by the study. Candidates who are in the process of completing their bachelor's degree have a six-month grace period from their hire date (up to one year if starting on a per diem basis) to provide degree equivalency verification.
Requirements
- Bachelor's Degree Related Field of Study required
- Some relevant research project work 0-1 year preferred
- Careful attention to detail and good organizational skills.
- Ability to follow directions.
- Good interpersonal and communication skills.
- Computer literacy.
- Working knowledge of clinical research protocols.
- Ability to demonstrate respect and professionalism for subjects' rights and individual needs.
Responsibilities
- Reviews proposals for compliance with sponsor and organizational guidelines; verifies that all sponsor requirements are met.
- Recruiting patients for clinical trials and conducting phone interviews.
- Verifies the accuracy of study forms and updates them per protocol.
- Prepares data for analysis and data entry.
- Documents patient visits and procedures.
- Assists with regulatory binders and QA/QC Procedures.
- Assists with interviewing study subjects.
- Assists with study regulator submissions.
Benefits
- comprehensive benefits
- career advancement opportunities
- differentials
- premiums
- bonuses
- recognition programs
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What This Job Offers
Job Type
Full-time
Career Level
Entry Level
