Clinical Research Coordinator

About the Role

The Clinical Research Coordinator I, under the supervision of the Principal Investigator, will apply state-of-the-art integrated PET and MRI and/or PET and CT imaging methods. This role involves acquiring and analyzing data, administrative coordination, and working with chronic pain patient populations. The goal of the research project is to evaluate the role of brain inflammation in the establishment and/or maintenance of persistent pain disorders.

Key Responsibilities

• Applying PET and MRI and/or PET and CT imaging methods.
• Acquiring and analyzing data.
• Administrative coordination.
• Working with different chronic pain patient populations.
• Preparing interim and annual reports.
• Preparing 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.
• Providing assistance on clinical research studies following established policies, procedures, and study protocols.
• 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.
• Maintaining and updating data generated by the study.
• 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.

Requirements & Tech Stack

• PET and MRI
• PET and CT
• Phlebotomy
• EKGs
• Regulatory binders
• QA/QC Procedures
• Study regulator submissions

Qualifications

Education

• Bachelor's Degree in a Related Field of Study required.

Experience

• 0-1 year of relevant research project work preferred.

Can this role accept experience in lieu of a degree? Yes

Knowledge, Skills and Abilities

• Careful attention to detail.
• 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 Details

• Work Location: 149 Thirteenth Street Building 149
• Scheduled Weekly Hours: 40
• Employee Type: Regular
• Work Shift: Day
• Pay Range: $21.00 - $29.01/Hourly