Senior Clinical Trials Coordinator – Oncology Research

University of California - San Diego Medical Centers; San Diego (CA); On-site; USD 94,000 - 151,000; Full time

Job summary

University of California - San Diego Medical Centers is seeking a Clinical Research Coordinator III to independently coordinate and oversee clinical research efforts for advanced trials. The role involves leadership of junior coordinators and ensuring rigorous protocol compliance and data integrity.

You will coordinate patient eligibility screening, consent, data collection, adverse event reporting, and regulatory submissions, while collaborating with principal investigators and disease groups.

Qualifications

• Experience with IRB submissions and regulatory documentation.
• Experience managing clinical trials and coordinating across teams.
• Proficient in data collection, entry, and analysis for trials.
• Negotiation of budgets related to clinical trial agreements.
• Understanding of FDA policies regulating clinical trials.
• Excellent written and verbal communication to interact with investigators and teams.

Responsibilities

• Coordinate and monitor multiple clinical trials from start-up through close-out.
• Provide leadership to junior coordinators and support staff.
• Ensure protocol compliance, data integrity, and safety reporting (AE/SAE).
• Manage regulatory submissions and trial start-up procedures; track invoicing and budgeting.

Skills

IRB processes

Clinical trials

Data management

Budget negotiations

FDA regulations

Communication skills

Education

Bachelor's degree

Job description

University of California - San Diego Medical Centers is seeking a Clinical Research Coordinator III to independently coordinate and oversee clinical research efforts for advanced trials. The role involves leadership of junior coordinators and ensuring rigorous protocol compliance and data integrity.

You will coordinate patient eligibility screening, consent, data collection, adverse event reporting, and regulatory submissions, while collaborating with principal investigators and disease groups.