Temple University's Clinical Research Department is searching for a Clinical Research Coordinator!
JOB POSTING BENEFITS AND SALARY:
Become a part of the Temple family and you will have access to the following:
A hybrid work schedule
Full medical, dental, vision coverage
Paid time off
12 Paid Holidays
Tuition remission - eligible employees and their dependents can obtain a degree TUITION FREE
A generous retirement plan and so much more!
Salary Range: $41,250-$55,000
A variety of important factors are reviewed by HR when considering salary, including job duties, the applicant's education and experience, all relevant internal equity considerations, department budget, and funding source.
Position Summary: The Clinical Research Coordinator, under the direction of the Director, CRORA and Clinical Investigators, will be responsible for the planning, implementation, and execution of Clinical Research studies in one or more departments in the Lewis Katz School of Medicine at Temple University. Incumbents will work independently to drive day-to-day research activities from study start-up to closeout.
* Must be available on nights and weekends when needed.
* This position requires the following background checks: criminal history review, child abuse clearance and FBI fingerprinting.
* There may be an opportunity for a hybrid work schedule depending on the department and study-specific needs.
REQUIRED AND PREFERRED
Required Education and Experience:
* Bachelor's degree in life science or health professions field
* At least three years of directly related clinical research coordinator experience
* An equivalent combination of education and experience may be considered.
Preferred Education and Experience:
*Prior phlebotomy certification or willingness to learn
*Prior research experience in a healthcare setting
*Prior research experience with NIH-sponsored research studies, industry clinical trials, and investigator-initiated research studies.
Required Skills and Abilities:
*Must have strong written and verbal communication skills with the ability to interact with a diverse population of students, faculty, staff, sponsors, and research participants.
*Ability to operate all standard office equipment/software, including MS Office.
*Ability to work independently or as a team with excellent attention to detail and adherence to project deadlines.
*Knowledge of FDA, IRB, Pennsylvania, and related regulations.
Preferred Skills and Abilities:
*Prior experience with IRB submissions, both local and central.
*Prior experience processing and shipping biological samples is a plus
*Prior experience with RedCap, OnCore CTMS, Epic Research, and Florence eBinders
*Prior Electronic Data Capture (eDC) data entry skills.
ADDITIONAL INFORMATION
Essential duties:
* Coordinate recruitment and enrollment of research participants;
* Establish and maintain databases of subjects;
* Schedule and conduct study visits;
* Collect and enter data; register subjects and study visits in OnCore;
* Perform Epic research billing review;
* Maintain an up-to-date regulatory binder;
* Schedule and attend sponsor visits; and prepare and submit IRB paperwork to ensure compliance with IRB regulations.
* Incumbent may assist with grant or manuscript preparation and
* Maintenance of investigator-initiated studies registered on clinicaltrials.gov;
* Support multiple active protocols simultaneously;
* Work with multiple investigators while adhering to the FDA, IRB, Pennsylvania, and related regulations.
Hybrid work schedule clause:
This position is assigned a hybrid work arrangement (on-campus and remote), the duration of this hybrid work arrangement is at the discretion of Temple University and the Department.
EEO, COMPLIANCE AND SAFETY REPORT
Temple University is committed to a policy of equal opportunity for all in every aspect of its operations, including employment, service, and educational programs. The University has pledged not to discriminate on the basis of age, color, disability, marital status, national origin or ethnic origin, race, religion, sex (including pregnancy), sexual orientation, gender identity, genetic information or veteran status.
Compliance Statement: In the performance of their functions as detailed in the position description employees have an obligation to avoid ethical, legal, financial and other conflicts of interest to ensure that their actions and outside activities do not conflict with their primary employment responsibilities at the institution. Employees are also expected to understand and be in compliance with applicable laws, University and employment policies and regulations, including NCAA regulations for areas and departments which their essential functions cause them to interact.
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