Research Coordinator I/II - Lung Cancer
Company: Cleveland Clinic
Location: Cleveland
Posted on: May 28, 2023
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Job Description:
Join the Cleveland Clinic team, where you will work alongside
passionate caregivers and provide patient-first healthcare.
Cleveland Clinic is recognized as the No. 4 hospital in the nation,
according to the U.S. and World News Report. 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.
Join our team as a Research Coordinator. You will get to join a
multi-disciplinary, talented team and work on studies that impact
future patient diagnoses and treatments. As a Research Coordinator,
you will coordinate the compliant implementation and conduct of
human subject research projects, typically of medium workload and
medium complexity. This role will support the lung cancer/lung
nodule research program. You may need to travel locally to regional
hospitals.
The future caregiver is someone who:
-Has research and clinical experience.
-Has High-level management and leadership skills.
-Is experience with conflict resolution and problem-solving.
-Has written and verbal communication skills.
-Has organizational and multitasking skills.
This is a rewarding opportunity that offers growth-oriented
projects, mentorship, support, and resources. You will experience
great exposure to both the institute and department leadership and
have numerous opportunities for career growth in different
administrative and project/program management
At Cleveland Clinic, we know what matters most. That is 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 will 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 will 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. roles. We will hire at the Research
Coordinator I or II level, depending on the candidate's experience.
Occasional travel to both Fairview Hospital and Hillcrest Hospital
will be required for this role.Phlebotomy experience preferred for
this position.
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.
Research Coordinator I Requirements
Education:
High School Diploma or GED. Associate's or Bachelor's degree in
health care or science related field preferred. Degree may offset
experience requirement.
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.
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.
Work Experience:
Minimum 2 years clinical research or healthcare experience
required.
Associate's or Bachelor's degree in healthcare or science field may
offset experience requirement.
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.
Research Coordinator II Requirements
Education:
High School Diploma or GED. Associate's or Bachelor's degree in
health care or science-related field preferred.
Bachelor's degree in healthcare or science field may offset two
years of experience requirement.
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.
Continually demonstrates competency with defined requirements for
the position as established by Cleveland Clinic. Education
preference.
Work Experience:
Certifications:
Complexity of Work:
Requires independent thinking skills, decisive judgment and the
ability work with minimal supervision.
Must be able to work in a stressful environment and take
appropriate action.
Physical Requirements:
A high degree of dexterity to produce materials on a computer.
Requires normal or corrected vision and hearing to normal
range.
Extensive sitting and frequent walking, occasional lifting or
carrying up to 25 pounds.
May have some exposure to communicable diseases or body fluids.
May require working irregular hours.
Personal Protective Equipment:
Follows standard precautions using personal protective equipment as
required.
May require working irregular hours.
Cleveland Clinic Health System is pleased to be an equal employment
employer: Women / Minorities / Veterans / Individuals with
Disabilities
Keywords: Cleveland Clinic, Cleveland , Research Coordinator I/II - Lung Cancer, Other , Cleveland, Ohio
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