Clinical Research Coordinator- Pulmonary Critical Care and Sleep

Screen reader users may encounter difficulty with this site. For assistance with applying, please contact [click to reveal email address] View email address on us.fitly.work . If you have questions while submitting an application, please review these frequently asked questions.

Current Employees and Students:

If you are currently employed or enrolled as a student at The Ohio State University, please log in to Workday to use the internal application process.

Welcome to The Ohio State University's career site. We invite you to apply to positions of interest. In order to ensure your application is complete, you must complete the following:

• Ensure you have all necessary documents available when starting the application process. You can review the additional section on postings for documents that may be required.
• Prior to submitting your application, please review and update (if necessary) the information in your candidate profile as it will transfer to your application.

Job Title:
Clinical Research Coordinator- Pulmonary Critical Care and Sleep

Department:
Medicine | IM Pulmonary Critical Care and Sleep

Clinical Research Coordinator to coordinate and perform daily clinical research activities in accordance with approved protocols administered by the non-cancer College of Medicine (COM) Center for Clinical Research Management (CCRM) for the Critical Care Trials Group in the Division of Pulmonary Critical Care in the Department of Internal 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, evaluates and calculates standardized scoring of diagnostic, psychological or behavioral testing or 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 equivalent combination of education experience required.

Required Experience

1 year of relevant experience required.

Preferred Experience

2-4 years of relevant experience preferred. Experience or knowledge in the relevant specialty area is preferred, and familiarity with medical terminology is desired. Clinical research certification from an accredited agency is considered an asset. Proficient computer skills are essential, including experience with Microsoft applications.

Requires successful completion of a background check; qualified candidates may be asked to complete a pre-employment physical, including a drug screen.

Function: Research and Scholarship

Subfunction: Clinical Research

Band: Individual Contributor Series-Specialized

Level: S2 Experienced

Additional Information:

This is a patient facing role and is required to work on site at the University Hospital at The Ohio State University.

Evening, weekend, holiday, and on-call hours are expected. Some travel to other OSU locations within the Columbus Metropolitan area may be required. Locations include, Dublin, New Albany, East Hospital, Outpatient East, Powell, and Martha Morehouse Pavillion.

Location:
Optometry Clinic (1041)

Position Type:
Regular

Scheduled Hours:
40

Shift:
First Shift

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

Thank you for your interest in positions at The Ohio State University and Wexner Medical Center. Once you have applied, the most updated information on the status of your application can be found by visiting the Candidate Home section of this site. Please view your submitted applications by logging in and reviewing your status. For answers to additional questions please review the frequently asked questions.

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