Research Coordinator I NE

About the role

Cleveland Clinic Nevada specializes in collaborative care, providing the community with ongoing care, clinical research and access to no-cost partner resources and education services. Here, you will work alongside a passionate and dedicated team, receive endless support and appreciation, and build a rewarding career at one of the most respected healthcare organizations in the world.

Schedule

A caregiver in this position works days from 8:00 a.m. – 4:30 p.m.

Pay

Pay range: minimum hourly $20.77, maximum hourly $31.68. The pay range displayed on this job posting reflects the anticipated range for new hires. A successful candidate’s actual compensation will be determined after taking factors into consideration such as the candidate’s work history, experience, skill set and education. The pay range displayed does not include any applicable pay practices (e.g., shift differentials, overtime, etc.) or the value of Cleveland Clinic’s benefits package (e.g., healthcare, dental and vision benefits, retirement savings account contributions, etc.).

Responsibilities

• Enroll patients in clinical trials
• Conduct study visits
• Collect questionnaires with important study-related information
• Support research across cognitive, multiple sclerosis (MS), and movement disorders, with opportunities to work on interventional and observational studies
• Perform data entry
• Process lab samples
• Schedule study visits
• Conduct neurocognitive assessments
• Recruit patients
• Interact with study monitors
• Assist with coordinating the compliant implementation and conduct of human subject research projects
• Maintain regulatory documents and binders
• Conduct data management
• Complete IRB submissions and communicate with the research team
• Report and complete serious adverse events and/or safety logs
• Communicate with sponsors, monitors and research personnel to ensure all aspects of study compliance
• Collaborate with primary investigators, sponsors and research caregivers to plan, conduct and evaluate project protocols, including research subject recruitment
• Schedule pre-site selection visits, site initiation visits, webinars, monitoring and close-out visits
• Plan, conduct and evaluate project protocols and research subject recruitment
• Monitor and report project status and research data
• Complete regulatory documents, data capture, monitoring plans and protocol-related activities
• Assist with preparing and responding to audits and maintaining research tools
• Complete certification in Human Subjects Research as required by the Responsible Conduct of Research guidelines adopted by Cleveland Clinic

Requirements

• Minimum qualifications: 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; demonstrated proficiency with various computer-based skills (word processing, spreadsheets, databases, presentation software, data entry, and EPIC); understanding of the basic concepts of study design; within 90 days of hire, must successfully complete certification in Human Subjects Research as required by the Responsible Conduct of Research guidelines adopted by Cleveland Clinic; strong organizational, communication and interpersonal skills.
• Preferred qualifications: Associate’s or Bachelor’s Degree in a healthcare or a science-related field; experience in clinical or lab research; background in healthcare; background in psychology.
• Ability to perform work in a stationary position for extended periods
• Ability to operate a computer and other office equipment
• Ability to communicate and exchange accurate information
• In some locations, ability to move up to 25 pounds
• Follows standard precautions using personal protective equipment as required