Clinical Research Coordinator-Hematology

The Ohio State University Wexner Medical Center; Columbus (OH); Hybrid; USD 42,000 - 60,000; Full time

Job summary

The Ohio State University Wexner Medical Center in Columbus, OH is seeking a Clinical Research Coordinator in Hematology to coordinate daily activities under approved protocols. The role includes patient recruitment, consent, scheduling, sample handling, and data collection, with on-site responsibilities across the James Cancer Hospital facilities.

Qualifications include a Bachelor’s degree in a biological/health/social sciences field and at least one year of clinical research experience.

Qualifications

• One year of clinical research experience required.
• Bachelor’s degree in biological sciences, health sciences, social sciences or related field or equivalent combination.

Responsibilities

• Coordinate and perform daily clinical research activities per approved protocols.
• Recruit, interview and enroll patients; obtain informed consent and ensure consent process compliance.
• Monitor patients for adverse reactions and report to clinical staff and sponsors.
• Collect, extract and analyze clinical research data; generate reports to ensure data validity.

Skills

Clinical research experience

Microsoft Office

Education

Bachelor’s degree in biological sciences/health sciences/social sciences or related field

Job description

## Clinical Research Coordinator-HematologyApply: James Cancer Hospital and Solove Research Institute: Full time: Posted Yesterday: R159833Screen reader users may encounter difficulty with this site. For assistance with applying, please contact [e-mail]. 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 job description 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-Hematology## Department:Medicine | IM Hematology**Job Summary:**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 Classical Hematology Division 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 an equivalent combination of education and experience required. **Minimum Experience Required**One year experience in a clinical research capacity required. **Skills and/or Experience Preferred**Experience or knowledge in inflammatory bowel diseases such as Crohn's; knowledge of medical terminology desired; clinical research certification from an accredited certifying agency desired; 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 Research**CAREER BAND: Individual Contributor-Specialized**CAREER LEVEL: S2*## Additional Information:This is a patient facing position and staff are required to be on site.A valid driver's license or reliable transportation will be needed as there may be some travel to other locations in the Columbus Metropolitan Area; those areas include Dublin, Powell, New Albany, Main Campus, and Martha Morehouse Pavillion.## Location:James Cancer Hospital (0375)## Position Type:Regular## Scheduled Hours:40## **Shift:**First Shift