Research Coordinator II
72,475 a year
Behavioral Health Market Context
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Benefits
Health InsuranceDental Coverage
Job Description
services for the entire family. At Cleveland Clinic, you will receive strong support and recognition, collaborate with dedicated professionals and build a rewarding career with one of the world's most respected healthcare organizations.
As a Research Coordinator II for DDI, you play a critical role in documenting data, maintaining timely reports, preparing audits, and ensuring departmental compliance, directly supporting Cleveland Clinic's mission to conduct safe, ethical, and efficient research. In this role, you will serve as the operational backbone of the research program, protecting patients, maintaining protocol integrity, and ensuring meaningful outcomes. The program focuses on improving quality of life after cancer surgery and prioritizes patient-centered research, partnering with patients to incorporate their insights into study design and enhance the overall patient experience.
A caregiver in this role works days from 8:30 a.m. -- 5:00 p.m.
A caregiver who excels in this role will:
• Coordinate 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.
• Serve as a liaison between investigators, research personnel, outside study personnel and central research administration offices to assist in protocol interpretation, enrollment and safety questions.
• 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.
Minimum qualifications for the ideal future caregiver include:
• High School Diploma or GED and three years of experience as a Research Coordinator I or performing the role of a Research Coordinator I
• OR Associate's or Bachelor's degree in health care or science related and one year of experience as a Research Coordinator I or performing the role of a Research Coordinator I
• Proficient with computer-based skills such as word processing, spreadsheets, database and presentation software
• Understand basic concepts of study design
Preferred qualifications for the ideal future caregiver include:
• Associate or Bachelor's degree in health care or science related field
• Experience as a clinical research coordinator
Physical Requirements:
• 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
Personal Protective Equipment:
• Follows standard precautions using personal protective equipment as required.
Pay Range
Minimum Annual Salary: $47,530.00
Maximum Annual Salary: $72,475.00
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.). The pay range does not include the value of Cleveland Clinic's benefits package (e.g., healthcare, dental and vision benefits, retirement savings account contributions, etc.).
As a Research Coordinator II for DDI, you play a critical role in documenting data, maintaining timely reports, preparing audits, and ensuring departmental compliance, directly supporting Cleveland Clinic's mission to conduct safe, ethical, and efficient research. In this role, you will serve as the operational backbone of the research program, protecting patients, maintaining protocol integrity, and ensuring meaningful outcomes. The program focuses on improving quality of life after cancer surgery and prioritizes patient-centered research, partnering with patients to incorporate their insights into study design and enhance the overall patient experience.
A caregiver in this role works days from 8:30 a.m. -- 5:00 p.m.
A caregiver who excels in this role will:
• Coordinate 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.
• Serve as a liaison between investigators, research personnel, outside study personnel and central research administration offices to assist in protocol interpretation, enrollment and safety questions.
• 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.
Minimum qualifications for the ideal future caregiver include:
• High School Diploma or GED and three years of experience as a Research Coordinator I or performing the role of a Research Coordinator I
• OR Associate's or Bachelor's degree in health care or science related and one year of experience as a Research Coordinator I or performing the role of a Research Coordinator I
• Proficient with computer-based skills such as word processing, spreadsheets, database and presentation software
• Understand basic concepts of study design
Preferred qualifications for the ideal future caregiver include:
• Associate or Bachelor's degree in health care or science related field
• Experience as a clinical research coordinator
Physical Requirements:
• 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
Personal Protective Equipment:
• Follows standard precautions using personal protective equipment as required.
Pay Range
Minimum Annual Salary: $47,530.00
Maximum Annual Salary: $72,475.00
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.). The pay range does not include the value of Cleveland Clinic's benefits package (e.g., healthcare, dental and vision benefits, retirement savings account contributions, etc.).
Qualifications
- •High School Diploma or GED and three years of experience as a Research Coordinator I or performing the role of a Research Coordinator I
- •OR Associate's or Bachelor's degree in health care or science related and one year of experience as a Research Coordinator I or performing the role of a Research Coordinator I
- •Proficient with computer-based skills such as word processing, spreadsheets, database and presentation software
- •Understand basic concepts of study design
- •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
Benefits
- •Minimum Annual Salary: $47,530.00
- •Maximum Annual Salary: $72,475.00
- •The pay range displayed on this job posting reflects the anticipated range for new hires
- •The pay range displayed does not include any applicable pay practices (e.g., shift differentials, overtime, etc.). The pay range does not include the value of Cleveland Clinic's benefits package (e.g., healthcare, dental and vision benefits, retirement savings account contributions, etc.)
Responsibilities
- •As a Research Coordinator II for DDI, you play a critical role in documenting data, maintaining timely reports, preparing audits, and ensuring departmental compliance, directly supporting Cleveland Clinic's mission to conduct safe, ethical, and efficient research
- •In this role, you will serve as the operational backbone of the research program, protecting patients, maintaining protocol integrity, and ensuring meaningful outcomes
- •The program focuses on improving quality of life after cancer surgery and prioritizes patient-centered research, partnering with patients to incorporate their insights into study design and enhance the overall patient experience
- •A caregiver in this role works days from 8:30 a.m. -- 5:00 p.m
- •A caregiver who excels in this role will:
- •Coordinate 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
- •Serve as a liaison between investigators, research personnel, outside study personnel and central research administration offices to assist in protocol interpretation, enrollment and safety questions
- •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
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