Clinical Research Coordinator-Cardiovascular Medicine

Ohio State University; Columbus (OH); In loco; USD 52.000 - 75.000; Tempo pieno

Descrizione del lavoro

Ohio State University is seeking a Clinical Research Coordinator to coordinate and perform daily clinical research activities in accordance with approved protocols at the Center for Clinical Research Management (CCRM). The role involves identifying eligible participants, recruiting and enrolling patients, obtaining informed consent, and educating patients about study purposes.

Responsibilities include monitoring for adverse events, data collection and analysis, and ensuring strict regulatory

Competenze

• Bachelor’s degree required in Biological Sciences, Health Sciences, Social Sciences or related field.
• 1 year of relevant clinical research experience required.
• Preferred: 2–4 years of relevant experience.
• Knowledge of medical terminology desired; clinical research certification from ACRP or SOCRA desired; computer skills with Microsoft Office applications desired.

Mansioni

• Coordinate and perform daily clinical research activities according to approved protocols.
• Assess patient records to identify eligibility and recruit, interview, enroll participants.
• Obtain informed consent and ensure consent process complies with regulatory and sponsor requirements.
• Monitor patients for adverse reactions and report to appropriate clinical staff and sponsors.
• Collect, process, and analyze clinical research data; generate and review reports for data validity.
• Ensure compliance with IRB, FDA and sponsor regulations; assist with QA/CS reviews and regulatory submissions.

Conoscenze

Clinical research certification (ACRP/

Formazione

Bachelor’s degree in Biological Sciences, Health Sciences, Social Sciences or related medical field

Strumenti

Microsoft Office

Descrizione del lavoro

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 Cardiovascular Medicine 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 monitoringpatients 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. **Minimum Experience Required**1 year of relevant experience required. **Preferred Experience**2-4 years of relevant experience preferred.**Preferred Skills and Certification**Knowledge of medical terminology desired; clinical research certification from an accredited certifying agency desired (ACRP or SOCRA); computer skills required with experience using Microsoft Software applications desired. ***Requires successful completion of a background check. Qualified candidates may be requested to complete a pre-employment physical, including a drug screen.*** FUNCTION/SUBFUNCTION: Research and Scholarship/Clinical ResearchCAREER BAND: Individual Contributor- SpecializedCAREER LEVEL: S2## Additional Information:This is a patient facing position and is required to be on site. Occasional evenings and weekends may be required depending on the approved protocol requirements. Occasional travel may be required within the Columbus Metropolitan Area; locations may be Outpatient Dublin, New Albany, Upper Arlington, Powell, Martha Morehouse, Outpatient East.## Location:Davis Heart and Lung Research Institute (0113)## Position Type:Regular## Scheduled Hours:40## **Shift:**First Shift