Research Coordinator II/III - Pediatric Hematology Oncology
Company: Cleveland Clinic
Location: Cleveland
Posted on: May 27, 2023
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Job Description:
Join our team at Cleveland Clinic and experience world-class
healthcare at its best. Cleveland Clinic is named the No. 4
hospital in the United States according to the U.S. and World News
Report. At Cleveland Clinic, you will be part of a talented,
compassionate, and driven team of caregivers. You will work with
state-of-the-art technology and provide stellar patient care. At
Cleveland Clinic you will build a rewarding career with one of the
most respected healthcare organizations in the world.
As a Research Coordinator II or III, you will be at the forefront
of our cutting-edge research clinical trials where we focus on the
characterization, diagnosis, and treatment of various pediatric
hematology and oncological 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 candidate is someone who:
-Preferably has 3 years of human subject research experience or if
not, three years of being a Registered Nurse or Respiratory
Therapist.
-Excels working both independently and as part of a team.
-Has outstanding communication and customer service skills.
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.
Cleveland Clinic provides what matters most: career growth,
delivering world-class care to our patients, continuous learning,
exceptional benefits and working for an organization that offers
many long-term career paths. Join us and experience a culture where
opportunities to advance and the support to get there go
hand-in-hand. We will hire at level 2 or level 3, based on
candidate's experience.
Responsibilities:
Independently directs large, complex, multi-center clinical
research protocols/programs and 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, and the development of
data capture and monitoring plans.
May be responsible for reporting 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, and research personnel to
ensure all aspects of study compliance.
Serves 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 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 and may oversee 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.
Oversees and monitors research data to maintain quality.
Understands basic concepts of study design.
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 develop or 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.
Assists with the development of training and educational material
for assigned research protocols, and documents education as
needed.
Conducts and documents the informed consent process.
Assists PI with research study design and development of research
protocol.
May submit the study to appropriate agencies in support of the
research programs and assist with annual and other reporting
requirements.
Will contribute to or assist with research project budget
development.
Performs other duties as assigned.
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.
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:
Research Coordinator III Requirements:
Education:
High School Diploma or GED. Associate's or Bachelor's degree in
health care or science related field strongly preferred.
Bachelor's degree may offset two years of 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:
Certifications:
Complexity of Work:
Is self-directed in planning, prioritizing and performing job
requirements with minimal supervision.
Exhibits the desire to expand job knowledge and skills through
training and skill development.
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:
Cleveland Clinic Health System is pleased to be an equal employment
employer: Women / Minorities / Veterans / Individuals with
Disabilities
Keywords: Cleveland Clinic, Cleveland , Research Coordinator II/III - Pediatric Hematology Oncology, Healthcare , Cleveland, Ohio
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