The Temple University's Lewis Katz School of Medicine's Research Administration Department is searching for a Sr. Clinical Research Coordinator-Pool 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: T26 Learn more about the "T" salary structure.
Salary Range: Up to $75,000.00 per year 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 position will be on-site *This position requires the following background checks: Child Abuse Certification and Cash Handling
Position Summary: The Senior Clinical Research Coordinator-Pool works under the direction of the Director, CRORA, 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 Senior 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 life science or health professions field and four years of directly related clinical research coordinator experience. *An equivalent combination of education and experience may be considered.
Responsibilities: The Senior Clinical Research Coordinator independently manages complex study coordination tasks, providing guidance on protocol implementation and regulatory compliance. This role involves making high-level decisions that require a broad interpretation of policies, procedures, and regulatory requirements to optimize study outcomes and maintain the highest standards of quality and compliance.
*Leads and manages the day-to-day operations of all assigned research projects and clinical trials, ensuring study milestones and timelines are met. *Independently screens, tracks, and enrolls patients in clinical trials and other research studies at the Lewis Katz School of Medicine at Temple University; coordinates and attends sponsor visits and site audits. *Enrolls human subjects for clinical trials; obtains informed consent, schedules and conducts complex clinical assessments, and ensures accurate and timely data collection and entry. *Organizes, maintains, and ensures accuracy of all documentation required for clinical trials and other research projects. May maintain up-to-date and audit-ready regulatory binders. *Serves as a primary resource to the Principal Investigator regarding patient responses to treatment, medication administration, and adverse events; identifies and escalates complex issues. *May prepare, review, and submit IRB and regulatory paperwork, ensuring full compliance with institutional, FDA, IRB, and state requirements; supports complex filings and amendments. *Assists the Principal Investigator with strategic planning for IRB submissions, a