Join the Cleveland Clinic team, where you will work alongside passionate caregivers and provide patient-first healthcare. Cleveland Clinic is recognized as one of the top hospitals in the nation. At Cleveland Clinic, you will work alongside passionate and dedicated caregivers, receive endless support and appreciation, and build a rewarding career with one of the most respected healthcare organizations in the world.As a Research Coordinator, you will be at the forefront of our cutting-edge research clinical trials where we focus on the characterization, diagnosis, and treatment of various respiratory diseases and conditions. You'll be able to assist with the study design and protocol development as well as directly interact with our patients daily. Your other duties will include but are not limited to:
Directing large, complex, multi-center clinical research protocols and programs.
Communicating with sponsors, monitors, and research personnel.
Collaborating with the primary investigator, sponsor and research staff to plan, conduct and evaluate protocols.
Developing and maintaining research tools, such as spreadsheets and questionnaires.
Maintaining Institutional Review Board submissions and communication with the team on that process.
Our ideal caregiver is someone who:
Exhibits the desire to expand job knowledge and skills through training and skill development.
Excels working both independently and as part of a team.
Has outstanding communication and customer service skills.
Has a flexible schedule. This position will require at least one weekend per month and some evening hours.
This opportunity is a great way to further develop your career in research and gain leadership skills, as this position is a step before moving into a supervisor role. By being involved in the research and the patients directly, you'll be exposed to many different teams and institutes, preparing you to further your career in other areas as well.At Cleveland Clinic, we know what matters most. That's why we treat our caregivers as if they are our own family, and we are always creating ways to be there for you. Here, you'll find that we offer: resources to learn and grow, a fulfilling career for everyone, and comprehensive benefits that invest in your health, your physical and mental well-being and your future. When you join Cleveland Clinic, you'll be part of a supportive caregiver family that will be united in shared values and purpose to fulfill our promise of being the best place to receive care and the best place to work in healthcare.We will hire at the I or II level, based on the candidate's level of experience.Responsibilities:
Coordinates the implementation and conduct of research projects ensuring adherence to research protocol requirements which may include: maintenance of regulatory documents and binders, data management, IRB submissions and communication of such to the research team.
May be responsible for reporting/completion of Serious Adverse Events and/or safety log as defined per protocol as they occur and completion of Food and Drug Administration (FDA) and sponsor forms in accordance with GCP guidelines.
Communicates with sponsors, monitors, research personnel to ensure all aspects of study compliance.
May 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.
Collaborates with study team to schedule pre-site selection visits, site initiation visits, webinars, monitoring and close-out visits.
Collaborates with primary investigator, sponsor and research staff to plan, conduct and evaluate project protocols, including research subject recruitment.
Monitors and reports project status.
Completes regulatory documents, data capture and monitoring plans.
Completes protocol related activities.
As delegated, may be required to attain and maintain clinical competencies for unlicensed caregivers such as phlebotomy, vital signs, ECG, POC testing and other testing as required.
Monitors research data to maintain quality.
Understands basic concepts of study design.
Demonstrates comprehension of assigned research protocols.
Develops and maintains knowledge of research protocol to coordinate the comprehensive and compliant execution of assigned protocols.
Assists with preparation for audits and response to audits.
May assist in the development and maintenance of research tools, such as spreadsheets, questionnaires and/or brochures.
Maintains study personnel certification records (License, CV, CITI).
Maintains professional relationships, including frequent and open effective communication with internal and external customers.
Documents the education and training of research personnel as needed.
May participate in the conduct and documentation of the informed consent process.
May assist PI with research study design and development of the research protocol.
May contribute to research project budget development.
Performs other duties as assigned.
Education:
High School Diploma or GED required.
Associate's or Bachelor's degree in health care or science related field preferred.
Associate's or Bachelor's degree in health care or science related field may substitute for two years of experience requirement.
Languages:
Language required
Language preferred
Certifications:
None required.
Complexity of Work:
Demonstrated proficiency with a variety of computer-based skills, especially in the use of word processing, spreadsheets, database and presentation software, and the ability to undertake internet searches.
Solid written and verbal communication skills.
Must be self-directed with demonstrated ability to work in collaboration and cooperation with members of a multidisciplinary team.
Continually demonstrates competency with defined requirements for the position as established by Cleveland Clinic. Education preference.
Work Experience:
Minimum three years' experience as a Research Coordinator I or performing the role of a Research Coordinator I. Associate's or Bachelor's degree in health care or science related field may offset two years of experience requirement.
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.
May require working irregular hours.
Personal Protective Equipment:
Follows standard precautions using personal protective equipment as required.
Pay RangeMinimum hourly: $22.85Maximum hourly: $34.85The pay range displayed on this job posting reflects the anticipated range for new hires. While the pay range is displayed as an hourly rate, Cleveland Clinic recruiters will clarify whether the compensation is hourly or salary. 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. This is not inclusive of the value of Cleveland Clinic's benefits package, which includes among other benefits, healthcare/dental/vision and retirement.Cleveland Clinic Health System is pleased to be an equal employment employer: Women / Minorities / Veterans / Individuals with Disabilities
