Clinical Research Coordinator A/B (Department of Cardiovascular Surgery)
Company: University of Pennsylvania
Location: Philadelphia
Posted on: April 25, 2025
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Job Description:
Clinical Research Coordinator A/B (Department of Cardiovascular
Surgery)
University Overview
The University of Pennsylvania, the largest private employer in
Philadelphia, is a world-renowned leader in education, research,
and innovation. This historic, Ivy League school consistently ranks
among the top 10 universities in the annual U.S. News & World
Report survey. Penn has 12 highly-regarded schools that provide
opportunities for undergraduate, graduate and continuing education,
all influenced by Penn's distinctive interdisciplinary approach to
scholarship and learning. As an employer Penn has been ranked
nationally on many occasions with the most recent award from Forbes
who named Penn one of America's Best Large Employers in 2023.
Penn offers a unique working environment within the city of
Philadelphia. The University is situated on a beautiful urban
campus, with easy access to a range of educational, cultural, and
recreational activities. With its historical significance and
landmarks, lively cultural offerings, and wide variety of
atmospheres, Philadelphia is the perfect place to call home for
work and play.
The University offers a competitive benefits package that includes
excellent healthcare and tuition benefits for employees and their
families, generous retirement benefits, a wide variety of
professional development opportunities, supportive work and family
benefits, a wealth of health and wellness programs and resources,
and much more.
Posted Job Title
Clinical Research Coordinator A/B (Department of Cardiovascular
Surgery)
Job Profile Title
Clinical Research Coordinator A
Job Description Summary
CRC A: The clinical research coordinator will be responsible for
data entry, organizing, maintaining, and assuring the accuracy of
all study documentation. The coordinator will oversee 2 or more
clinical trial ensuring that the integrity of the protocol is
maintained, all data and queries are answered in a timely manner,
appropriate AEs and SAEs are reported to the sponsor and IRB per
protocol. The CRC will participate in clinic to explain the trial
to the patient and family, enroll and consent patients and complete
any follow-up or research activity required. All communication with
the participant or on behalf of the participant must be documented
in PennChart. The CRC will be responsible for gather the data per
the protocol and bring any adverse events to the attention of the
PI or any other part of the research team that the PI delegates the
task. The CRC will work closely with the administrative assistant
to ensure that study visits are scheduled along with the
appropriate studies according to the protocol. The CRC will conduct
phone interviews if necessary. The CRC must complete relevant
training to function in the role including electronic databases,
processing and shipping specimens and phlebotomy. The CRC will
maintain all mandatory trainings required to oversee and manage the
trials which they are the lead CRC or backup CRC. The CRC will
report directly to the Project Manager or the program Supervisor.
The CRC must be sufficiently knowledgeable about Microsoft word,
Excel, and other standard programs. The CRC must maintain
professionalism and follow the guidelines of the institution.
CRC B: The CRC B will have all of the same responsibilities as a
CRC A with added responsibilities and better knowledge base of
clinical research. A CRC B is expected to manage 5 or more clinical
trials. The CRC B will be well versed in Good Clinical Practice.
The CRC B will have experience in managing all aspects of a trial
including trial start-up, creating consents, IRB submissions,
recruitment, enrollment, AE management, investigational and drug
management, data entry, resolution of queries, strategies to
maintain compliance and closeout of a trial. The CRC B will be able
to effectively manage multiple trials and assist in aspects of
other trials. The CRC B will demonstrate leadership skills within
the program and be able to identify common challenges and
brain-storm creative ideas to problem-solve issues.
The CRC will update the PI and Subs of all protocol modifications,
AEs, SAEs and deviations related to the protocol. The CRC will
document education and notification of protocol related
information. The CRC B will educate subjects and the family of
potential participates in the trial which includes the device/drug,
procedure and follow up to ensure informed consent is obtained. All
interaction must be documented in PennChart. In the event a subject
is unable to return for their study visit the CRC will contact the
subject and investigate the barriers and problem-solve possible
solutions.
The CRC must be sufficiently knowledgeable about Microsoft word,
Excel, and other standard programs. The CRC must maintain
professionalism and follow the guidelines of the institution.
This position is contingent upon continued grant funding.
Qualifications:
CRC A: Bachelor of Science and 1 to 2 years of experience or
equivalent combination of education and experience is required.
CRC B: Bachelor of Science and 2 to 3 years of experience or
equivalent combination of education and experience is required.
Job Description
CRC A: The clinical research coordinator will be responsible for
data entry, organizing, maintaining, and assuring the accuracy of
all study documentation. The coordinator will oversee 2 or more
clinical trial ensuring that the integrity of the protocol is
maintained, all data and queries are answered in a timely manner,
appropriate AEs and SAEs are reported to the sponsor and IRB per
protocol. The CRC will participate in clinic to explain the trial
to the patient and family, enroll and consent patients and complete
any follow-up or research activity required. All communication with
the participant or on behalf of the participant must be documented
in PennChart. The CRC will be responsible for gather the data per
the protocol and bring any adverse events to the attention of the
PI or any other part of the research team that the PI delegates the
task. The CRC will work closely with the administrative assistant
to ensure that study visits are scheduled along with the
appropriate studies according to the protocol. The CRC will conduct
phone interviews if necessary. The CRC must complete relevant
training to function in the role including electronic databases,
processing and shipping specimens and phlebotomy. The CRC will
maintain all mandatory trainings required to oversee and manage the
trials which they are the lead CRC or backup CRC. The CRC will
report directly to the Project Manager or the program Supervisor.
The CRC must be sufficiently knowledgeable about Microsoft word,
Excel, and other standard programs. The CRC must maintain
professionalism and follow the guidelines of the institution.
CRC B: The CRC B will have all of the same responsibilities as a
CRC A with added responsibilities and better knowledge base of
clinical research. A CRC B is expected to manage 5 or more clinical
trials. The CRC B will be well versed in Good Clinical Practice.
The CRC B will have experience in managing all aspects of a trial
including trial start-up, creating consents, IRB submissions,
recruitment, enrollment, AE management, investigational and drug
management, data entry, resolution of queries, strategies to
maintain compliance and closeout of a trial. The CRC B will be able
to effectively manage multiple trials and assist in aspects of
other trials. The CRC B will demonstrate leadership skills within
the program and be able to identify common challenges and
brain-storm creative ideas to problem-solve issues.
The CRC will update the PI and Subs of all protocol modifications,
AEs, SAEs and deviations related to the protocol. The CRC will
document education and notification of protocol related
information. The CRC B will educate subjects and the family of
potential participates in the trial which includes the device/drug,
procedure and follow up to ensure informed consent is obtained. All
interaction must be documented in PennChart. In the event a subject
is unable to return for their study visit the CRC will contact the
subject and investigate the barriers and problem-solve possible
solutions.
The CRC must be sufficiently knowledgeable about Microsoft word,
Excel, and other standard programs. The CRC must maintain
professionalism and follow the guidelines of the institution.
This position is contingent upon continued grant funding.
Qualifications:
CRC A: Bachelor of Science and 1 to 2 years of experience or
equivalent combination of education and experience is required.
CRC B: Bachelor of Science and 2 to 3 years of experience or
equivalent combination of education and experience is required.
Job Location - City, State
Philadelphia, Pennsylvania
Department / School
Perelman School of Medicine
Pay Range
$46,500.00 - $55,000.00 Annual Rate
Salary offers are made based on the candidate's qualifications,
experience, skills, and education as they directly relate to the
requirements of the position, and in alignment with salary ranges
based on external market data for the job's level. Internal
organization and peer data at Penn are also considered.
Equal Opportunity Statement
The University of Pennsylvania is an equal opportunity employer.
Candidates are considered for employment without regard to race,
color, sex, sexual orientation, religion, creed, national origin
(including shared ancestry or ethnic characteristics), citizenship
status, age, disability, veteran status or any class protected
under applicable federal, state or local law.
Special Requirements
Background checks may be required after a conditional job offer is
made. Consideration of the background check will be tailored to the
requirements of the job.
University Benefits
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To learn more, please visit:
https://www.hr.upenn.edu/PennHR/benefits-pay
Equal Employment Opportunity Statement
The University of Pennsylvania is an equal opportunity employer.
Candidates are considered for employment without regard to race,
color, sex, sexual orientation, religion, creed, national origin
(including shared ancestry or ethnic characteristics), citizenship
status, age, disability, veteran status or any class protected
under applicable federal, state, or local law.
To apply, visit
https://wd1.myworkdaysite.com/en-US/recruiting/upenn/careers-at-penn/job/HUP/Clinical-Research-Coordinator-A-B--Department-of-Cardiovascular-Surgery-_JR00100835-1
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