The Temple University's Lewis Katz School of Medicine's TMS-Pulm/CriticalCare/SleepMed Department is searching for a Clinical Research Coordinator-Recruitment to join our team!
Become a part of the Temple family and you will have access to the following:
Full medical, dental, vision coverage
Paid time off
11 Paid Holidays
Tuition remission - eligible employees and their dependents can obtain a degree TUITION FREE
A generous retirement plan and so much more!
Salary Grade: T25
Learn more about the "T" salary structure
Salary Range: $50,000 to $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.
This role is also eligible for our employee referral program-TERP! Current employees can earn up to $500! Conditions apply. Please contact the HR Employment office for details.
Job Details:
*This is a grant-funded position
*This position requires the following background checks: Cash Handling
*Clinical Research Coordinators may be hired for a specific department or as a pooled coordinator.
*Hybrid work options may be considered depending on study and departmental needs.
Position Summary:
The Clinical Research Coordinator works under the leadership of the Principal Investigator and/or other Research Staff and is responsible for specific research tasks associated with clinical research projects or clinical trials, ensuring high-quality data collection, regulatory compliance, and seamless study operations.
As a Clinical Research Coordinator, you will also have the opportunity to advance your career through our structured step increase program. We also recognize and reward professional development. Coordinators who successfully earn industry-recognized certifications, such as the Certified Clinical Research Professional (CCRP®) through SOCRA or the Certified Clinical Research Coordinator (CCRC®) through ACRP, may qualify for advancement sooner.
At Temple University's Lewis Katz School of Medicine, you will be part of a nationally recognized, state-of-the-art research community that is driving innovation in patient care. Our clinical research programs span a wide range of disciplines and provide coordinators with the opportunity to contribute to groundbreaking studies that directly impact the health and well-being of diverse populations. With access to advanced resources, collaborative teams, and a strong commitment to excellence, Temple offers an ideal environment for Clinical Research Coordinators to grow their careers while shaping the future of medicine.
Required Education and Experience:
*Bachelor's degree in a life science or other health professions field
*A minimum of three years of related experience
*An equivalent combination of education and experience may be considered.
Responsibilities:
The Clinical Research Coordinator performs study coordination tasks independently, following established protocols and procedures. The coordinator makes decisions that require interpretation of policies, procedures, or instructions to ensure accurate and compliant execution of clinical research projects.
*Oversees the day-to-day activities of all assigned research projects and clinical trials.
*Screens, tracks, and enrolls patients in clinical trials and other research studies for the Lewis Katz School of Medicine at Temple University. Schedule and attend sponsor visits.
*Enrolls human subjects for clinical trials. Obtains informed consent, schedules subjects for visits, performs clinical assessments and collects and enters study data.
*Performs various research, database, and clerical tasks to support clinical trials, aiding investigators in organizing, gathering, and compiling clinical research data.
*Organizes and maintains documentation required for clinical trials and/or other research projects. Maintains up-to-date regulatory binders.
*Inform the Principal Investigator or designated individual about any issues regarding patient responses to treatment, medication, or adverse effects.
*May submit IRB paperwork to ensure compliance with IRB regulations.
*Assist the Principal Investigator with Institutional Review Board (IRB) filings and annual reviews.
*Offer clerical and technical support to ensure adherence to research protocols and maintain the quality of information received.
*May prepare, review, and submit IRB and regulatory paperwork