Clinical Research Coordinator B/C
Company: University of Pennsylvania
Location: Philadelphia
Posted on: April 25, 2025
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Job Description:
Clinical Research Coordinator B/C
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.
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 B/C
Job Profile Title
Clinical Research Coordinator B
Job Description Summary
This position's primary function is to facilitate, promote, and
ensure good clinical practice in the conduct of all research
protocols in the Department/Center. Manages different phases of
complex clinical trials and mentors Coordinators and Research
Assistants. Works with partnering institutions and creates
multi-center budgets and manages expenses. Participates in study
team meetings, disease site group meetings, and ongoing protocol
training/compliance meetings. Supports in the monitoring of
external sites and assists in the management of multi-site trials.
Adheres to all University and other regulatory guidelines.
Job Description
Clinical Research Coordinator B: With minimal supervision,
coordinate Phase I-IV clinical trials. Recruit, consent and screen
patients according to protocol. Schedule patient visits and any
necessary testing. Monitor patients per protocol requirements and
ensure adherence to protocol requirements. Organize and maintain
all documentation required by the sponsor or CRO- includes source
documentation, case report forms, and research charts. Collect,
review and report study data, complete case report forms and
resolve data queries, process and ship study specimens including
blood, urine and tissue samples, Participate in initiation,
monitoring, audit and close-out visits. Participate in study team
meetings, disease site group meetings, and ongoing protocol
training/compliance meetings. Assist in the development/maintenance
of study specific case report forms and source document tools, show
vigilance in patient safety, protocol compliance and data quality.
Assist in the monitoring of external sites and assist in the
management of multi-site trials. Adhere to all University of
Pennsylvania, FDA and GCP guidelines.
Clinical Research Coordinator C: Independently manage Phase I-IV
complex clinical trials, mentor coordinators and research
assistants, consent and screen patients according to protocol.
Schedule patient visits and any necessary testing. Monitor patients
per protocol requirements and ensure adherence to protocol
requirements, Organize and maintain all documentation required by
the sponsor or CRO - includes source documentation, case report
forms, and research charts. Collect, review and report study data,
complete case report forms and resolve data queries, process and
ship study specimens including blood, urine and tissue samples.
Participate in initiation, monitoring, audit and close-out visits,
Participate in study team meetings, disease site group meetings,
and ongoing protocol training/compliance meetings, Assist in the
development/maintenance of study specific case report forms and
source document tools. As needed, monitor external research sites
and manage various aspects of multi-site trials. Show vigilance in
patient safety, protocol compliance and data quality. Adhere to all
University of Pennsylvania, FDA and GCP guidelines.
Clinical Research Coordinator B - Bachelors Degree; 2-4 years
experience or equivalent combination of education and experience
required.
Clinical Research Coordinator C - Bachelors Degree; 4-6 years
experience or equivalent combination of education and experience
required.
Position contingent upon funding.
Job Location - City, State
Philadelphia, Pennsylvania
Department / School
Perelman School of Medicine
Pay Range
$42,953.00 - $77,315.00
Affirmative Action Statement
Penn adheres to a policy that prohibits discrimination on the basis
of race, color, sex, sexual orientation, gender identity, religion,
creed, national or ethnic origin, citizenship status, age,
disability, veteran status, or any other legally protected
class.
Special Requirements
Background check required after a conditional job offer is made.
Consideration of the background check will be tailored to the
requirements of the job.
University Benefits
To learn more, please visit:
https://www.hr.upenn.edu/PennHR/benefits-pay
To apply, visit
https://wd1.myworkdaysite.com/en-US/recruiting/upenn/careers-at-penn/job/Perelman-Center-for-Adv-Medicine/Clinical-Research-Coordinator-B-C_JR00012744
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