Clinical Research Coordinator I — Cardio Trials

Cleveland Clinic; Cleveland (OH); In loco; USD 29.000 - 44.000; Tempo pieno

Descrizione del lavoro

Cleveland Clinic’s Main Campus is seeking a Research Coordinator I to enroll patients in clinical trials, conduct study visits, collect questionnaires, and perform research procedures. You will interact with patients through screening and enrollment, coordinating visits, managing data, and ensuring study compliance. Training for phlebotomy and EKGs is provided. Hours are 8:30 a.m.

– 5:00 p.m. (flexible). Pay range is $20.77–$31.68 hourly, and benefits are included as part of the compensation

Competenze

• High School Diploma or GED and two years of clinical research or healthcare experience.
• OR Associate’s or Bachelor’s Degree in a healthcare or a science-related field.
• Proficiency with computer-based skills (word processing, spreadsheets, databases, presentation software, data entry) and EPIC.
• Within 90 days of hire, complete Human Subjects Research certification as required by Cleveland Clinic.
• Strong organizational, communication and interpersonal skills.

Mansioni

• Assist with coordinating compliant implementation of human subject research projects.
• Maintain regulatory documents and binders, conduct data management, and communicate with the research team.
• Report and complete serious adverse events and safety logs.
• Communicate with sponsors, monitors, and research personnel to ensure study compliance.
• Collaborate with PIs, sponsors, and research caregivers to plan and evaluate project protocols, including recruitment.
• Schedule site visits and webinars, monitoring visits, and close-out visits.
• Plan and evaluate project protocols and recruitment.
• Monitor and report project status and research data.
• Complete regulatory documents, data capture, monitoring plans, and protocol activities.
• Assist with audits and maintaining research tools.
• Screen patients for study eligibility and obtain informed consent.
• Perform phlebotomy for research purposes.
• Process blood and urine samples (training provided).
• Perform study procedures, including questionnaire administration, vital signs, and EKGs (training provided).
• Maintain study regulatory binders.

Conoscenze

Organizational skills

Communication

Interpersonal skills

Data management

Formazione

High School Diploma or GED

Associate’s or Bachelor’s Degree in healthcare or science

Strumenti

EPIC

Descrizione del lavoro

Cleveland Clinic’s Main Campus is seeking a Research Coordinator I to enroll patients in clinical trials, conduct study visits, collect questionnaires, and perform research procedures. You will interact with patients through screening and enrollment, coordinating visits, managing data, and ensuring study compliance. Training for phlebotomy and EKGs is provided. Hours are 8:30 a.m.

– 5:00 p.m. (flexible). Pay range is $20.77–$31.68 hourly, and benefits are included as part of the compensation