Clinical Research Coordinator

Clinical Research CoordinatorUnder the supervision of the Principal Investigator, the Clinical Research Coordinator applies state-of-the-art integrated PET and MRI and/or PET and CT imaging methods. Responsibilities include acquiring and analyzing data, administrative coordination, and working with different chronic pain patient populations. The incumbent prepares interim and annual reports, as well as reports of completed projects for publication in technical journals, presentations at professional field meetings/conferences, and for use in further applied or theoretical research activities. The goal of this research project is to evaluate the role of brain inflammation in the establishment and/or maintenance of persistent pain disorders.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.Essential Functions: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.Qualifications:Education: Bachelor's Degree related field of study required.Can this role accept experience in lieu of a degree? Yes.Licenses and Credentials: None required.Experience: Some relevant research project work 0-1 year preferred.Knowledge, Skills and Abilities: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.Additional Job Details (if applicable):Remote Type: OnsiteWork Location: 149 Thirteenth StreetScheduled Weekly Hours: 40Employee Type: RegularWork Shift: Day (United States of America)Pay Range: $21.00 - $29.01/HourlyEEO Statement:1200 The General Hospital Corporation is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religious creed, national origin, sex, age, gender identity, disability, sexual orientation, military service, genetic information, and/or other status protected under law. We will ensure that all individuals with a disability are provided a reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. To ensure reasonable accommodation for individuals protected by Section 503 of the Rehabilitation Act of 1973, the Vietnam Veteran's Readjustment Act of 1974, and Title I of the Americans with Disabilities Act of 1990, applicants who require accommodation in the job application process may contact Human Resources.