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University of Pennsylvania
Overview
The role involves coordinating complex oncology clinical trials, ensuring protocol execution according to GCP and HIPAA standards. Responsibilities include managing patient visits, handling regulatory submissions, and maintaining audit-ready study files.
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Compensation
$53,418 - $60,813 / YEAR
Posted
10 days ago
University of Pennsylvania Perelman School of Medicine
Coordinate and execute oncology clinical trials in accordance with GCP and HIPAA regulations. Manage patient eligibility, data collection, regulatory documentation, and biological sample processing.
Flourish Research
The coordinator executes protocol-specified patient visits and procedures while documenting study data in accordance with GCP and FDA guidelines. They are also responsible for recruiting qualified subjects, obtaining informed consent, and reporting adverse events to sponsors and investigators.
$31 - $43 / HOUR
14 days ago
United Urology Group
The Research Coordinator will screen, enroll, and follow study subjects for clinical trials, ensuring protocol compliance and monitoring. Responsibilities include conducting clinical trials, enrolling subjects, and managing follow-up procedures.
$27 - $31 / HOUR
25 days ago
Perelman School of Medicine at the University of Pennsylvania
The Clinical Research Coordinator will participate in and coordinate clinical trials within the Department of Medicine, supporting a diverse group of investigators. Responsibilities include study design, patient recruitment, regulatory compliance, and data management.
$46,500 - $67,046 / YEAR
1 month ago
HUCKEYE HEALTH SERVICES LLC
The Clinical Research Coordinator manages complex clinical trials including drug, device, and biologic studies across all phases. They work closely with physicians and stakeholders to ensure compliance with Good Clinical Practice and FDA regulations.
$48 / HOUR
2 months ago
Tribe513 | The Onyx Group
The Clinical Research Coordinator is primarily responsible for conducting Phase II, III, and IV clinical trials according to international standards, overseeing assigned trials under the direction of the Primary Investigator and Site Lead. Key duties include managing the informed consent process, medical record review, protocol compliance, patient relations, and administration of investigational products.
Salary not listed
OSF HealthCare
The Cardiac Rehab RN provides medical coverage for participants during Cardiac Rehabilitation Phase II & III exercises and education classes, and is responsible for medical coverage during Rapid Responses and Code Blue events within the rehabilitation department. This role functions as an active member of the interdisciplinary Cardiac Rehab team, collaborating with Exercise Specialists, Dieticians, Respiratory Therapy, and medical providers.
3 months ago
The Clinical Research Coordinator manages complex clinical trials including drug, device, and biologic studies across all phases. They work closely with study physicians and stakeholders to ensure compliance with Good Clinical Practice and FDA regulations.
$50 / HOUR
4 months ago
