Senior Clinical Research Coordinator - Oncology Trials

American Oncology Partners, PA; United States; On-site; USD 61,000 - 88,000; Full time

Benefits offered by this job

Health insurance

401(k) match

Paid time off (PTO)

Tuition assistance

Job summary

Oncology Consultants in the United States seeks a Senior Clinical Research Coordinator to oversee clinical trials from initiation to close-out. You will support investigators, ensure regulatory compliance, and mentor staff in data capture, safety reporting, and study documentation.

The role requires coordinating patient recruitment, conducting visits, and maintaining study records across multiple trials while communicating with sponsors, IRBs, and physicians.

Qualifications

• Education Degree in the life sciences or health sciences such as Registered Nurse (R.N.), bachelor's in science, Doctor in Philosophy (Ph.D.), Medical Doctorate (M.D.), other.
• Minimum Relevant Experience 5 plus years of clinical research experience.
• Certifications/Licenses Continuing education participation is expected, and research certification through a recognized national organization (SOCRA, ACRP) is encouraged. NIH protection of Human subjects online course will be required every 2 years. IATA training will be required every 2 years.

Responsibilities

• Study Start-Up & Regulatory Compliance: Responsible for study feasibility, regulatory submissions, and study initiation activities to ensure all clinical trials meet regulatory, IRB, and protocol requirements.
• Patient Recruitment, Enrollment & Study Coordination: Coordinate patient recruitment, enrollment, scheduling, and overall subject participation throughout the clinical trial.
• Clinical Trial Execution & Patient Care Activities: Provide direct patient care and coordinate all clinical and protocol-related procedures to ensure study compliance and patient safety.
• Data Management, Documentation & Monitoring Support: Maintain accurate study documentation, case report forms, and support sponsor monitoring and audit activities.
• Research Program Support, Communication & Project Coordination: Support research department operations, communication, reporting, and overall research program coordination.

Skills

Clinical research coordination

Regulatory compliance

Patient recruitment

Data management

Communication

Education

Life sciences degree

RN (Registered Nurse)

Bachelor of Science

PhD

MD

Job description

Oncology Consultants in the United States seeks a Senior Clinical Research Coordinator to oversee clinical trials from initiation to close-out. You will support investigators, ensure regulatory compliance, and mentor staff in data capture, safety reporting, and study documentation.

The role requires coordinating patient recruitment, conducting visits, and maintaining study records across multiple trials while communicating with sponsors, IRBs, and physicians.