Clinical Research Coordinator

Description

• Manage oncology research studies as a study coordinator.
• Ensure compliance with IRB and human research protection regulations.
• Report adverse events using CTCAE 4.0 and manage cancer medication protocols.
• Perform chart reviews and data entry following Good Clinical Practice (GCP) guidelines.
• Conduct patient enrollment, informed consent, and patient scheduling.
• Coordinate and manage clinical research projects, ensuring they meet established timelines and objectives.

Requirements

• Interact comfortably and professionally with physicians and other healthcare professionals.
• Knowledge of IRB and human research protection regulations.
• Experience with cancer medications and adverse event reporting preferred.
• Proficiency in MS Office Suite.
• Strong experience in oncology research and clinical coordination.
• Experience in lymphoma or oncology preferred.
• Minimum of two to three years of clinical research experience.

Benefits

• Employee Assistance Program
• Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a hybrid position in Philadelphia,PA. Application Deadline This position is anticipated to close on Dec 19, 2025.
• 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
• Critical Illness, Accident, and Hospital
• Transportation benefits
• Medical, dental & vision
• Health Spending Account (HSA)
• Short and long-term disability
• Life Insurance (Voluntary Life & AD&D for the employee and dependents)

Training + Development

Interview process

Visa Sponsorship

Security clearance