Clinical Research Coordinator - Emergency Medicine

The Ohio State University Wexner Medical Center; United States; On-site; USD 55,000 - 70,000; Full time

Job summary

The Ohio State University Wexner Medical Center is seeking a Clinical Research Coordinator for the Emergency Medicine department. The role involves coordinating daily clinical research activities, patient screening, consent, and scheduling, as well as data collection and regulatory compliance.

Responsibilities include monitoring for adverse reactions, data quality reviews, and contributing to protocol development and external quality assurance.

Qualifications

• Bachelor's Degree in biological sciences, health sciences, social sciences or other medical field (or equivalent combination of education and experience).
• One year experience in a clinical research capacity required.

Responsibilities

• Coordinate and perform daily clinical research activities in accordance with approved protocols.
• Identify eligible patients by reviewing records; recruit, interview and enroll participants; obtain informed consent and ensure compliant consent process.
• Coordinate scheduling and follow-through of appointments, procedures, and diagnostic testing per protocol.
• Assist with collection, processing and evaluation of biological samples; administer questionnaires.
• Monitor patients for adverse reactions, notify appropriate clinical professionals, and assist with data reporting and sponsor/regulatory communications.
• Assist with securing IRB/FDA compliance and prepare for external QA reviews; help develop new protocols and study goals.

Education

Bachelor's Degree in biological sciences, health sciences, social sciences or other medical field

Job description

Clinical Research Coordinator - Emergency Medicine

Department: Medicine | Emergency Medicine

Clinical Research Coordinator to coordinate and perform daily clinical research activities in accordance with approved protocols administered by the non-cancer Clinical Trials Management Organization for Department of Emergency Medicine assists with assessing patient records to identify patients who are eligible to participate in specified clinical research protocols; recruits, interviews and enrolls patients; obtains informed consent and ensures consent process is administered in compliance to regulatory and sponsor requirements; educates patients and families of purpose, goals, and processes of clinical study; coordinates scheduling and follow-through of patient care appointments, procedures, & other diagnostic testing in accordance with study protocol; participates in the collection, processing & evaluation of biological samples; administers questionnaires; assists with monitoring patients for adverse reactions to study treatment, procedure or medication and notifies appropriate clinical professional to evaluate patient response, identify status of complications, & provide appropriate level of care; documents unfavorable responses and notifies research sponsors & applicable regulatory agencies; participates in evaluating patients for compliance related to protocol; assists with collecting, extracting, coding, and analyzing clinical research data; generates reports and reviews to ensure validity of data; supports activities to ensure compliance with all Institutional Review Boards (IRB), FDA (Federal Drug Administration), federal, state and industry sponsor regulations; assists with coordinating and preparing for external quality assurance and control reviews by IRB, federal or industry sponsors; participates in activities to develop new research protocols and contributes to establishment of study goals to meet protocol requirements.

Minimum Education Required Bachelor's Degree in biological sciences, health sciences, social sciences or other medical field or an equivalent combination of education and experience required.

Minimum Experience Required One year experience in a clinical research capacity required.

Additional Information

Location: Prior Hall (0302)

Position Type: Regular

Scheduled Hours: 40

Shift: Varying Shifts

Final candidates are subject to successful completion of a background check. A drug screen or physical may be required during the post offer process.

The university is an equal opportunity employer, including veterans and disability.

Ohio State benefits give you options to take care of what matters most to you - and opportunities to make adjustments as your life and needs change, including:

• Medical, dental and vision coverage, with Ohio State paying a significant portion of the cost.
• Paid time off, including sick and vacation time and 11 holidays.
• State retirement plan or an alternative retirement plan, both with generous employer contributions.

As Buckeyes, we accomplish more together. No matter your role, you'll be part of creating what people need now: pathways to education, research and health care. Working at Ohio State means you're part of a team with a strong sense of community and an unwavering commitment to excellence - and, of course, incomparable Buckeye spirit. We bring out the best in people, help each other succeed and learn together. By joining Ohio State, you become part of a top-20 public university with one of America's leading academic health centers. We're a team of dedicated colleagues with access to boundless resources that support you.