Cancer Research Coordinator: Clinical Trials & Patient Care

Ohio State University; Columbus (OH); On-site; USD 52,000 - 76,000; Full time

Benefits offered by this job

Medical, dental, and vision coverage

Paid time off (sick, vacation, 11 paid

Holidays

Retirement plan with employer matching

Job summary

The Ohio State University Wexner Medical Center seeks a Clinical Research Coordinator to manage daily clinical research activities within the Recruitment, Intervention and Survey Shared Resource of the Comprehensive Cancer Center.

The role involves assessing patient records for trial eligibility, enrolling participants, obtaining informed consent, educating participants, scheduling visits, monitoring adverse events, and ensuring compliance with IRB, FDA and sponsor regulations.

Qualifications

• Bachelor's Degree in biological, health, social sciences or related field required.
• One year of clinical research experience required.
• Knowledge of medical terminology desirable.
• Clinical research certification desirable.
• Computer skills with Microsoft Office desired.
• Excellent written and spoken communication with staff, participants and collaborators.

Responsibilities

• Identify eligible patients by reviewing records for specified protocols.
• Recruit, interview and enroll participants for trials.
• Obtain informed consent per regulatory and sponsor requirements.
• Educate patients and families about study purpose and procedures.
• Coordinate scheduling of appointments, procedures and tests per protocol.
• Monitor patients for adverse reactions and escalate as needed.
• Document data and report unfavorable responses to sponsors and IRBs.

Skills

Communication skills

Medical terminology

MS Office proficiency

Education

Bachelor's Degree in biological/health sciences or equivalent

Tools

MS Office

Job description

The Ohio State University Wexner Medical Center seeks a Clinical Research Coordinator to manage daily clinical research activities within the Recruitment, Intervention and Survey Shared Resource of the Comprehensive Cancer Center.

The role involves assessing patient records for trial eligibility, enrolling participants, obtaining informed consent, educating participants, scheduling visits, monitoring adverse events, and ensuring compliance with IRB, FDA and sponsor regulations.