Senior Clinical Research Coordinator - Multi-Study Impact

Stanford Reglab; Palo Alto (CA); On-site; USD 85,000 - 110,000; Full time

Job summary

Stanford Radiology in Palo Alto is seeking a Senior Clinical Research Coordinator (CRC2) to support multiple studies under the Investigator and Clinical Research Manager. You will develop recruitment strategies, oversee study operations, ensure regulatory compliance, and manage project progress.

The successful candidate will have strong communication and organizational skills, experience in clinical research, and the ability to handle shifting priorities while working with investigators,

Qualifications

• Investigator Initiated clinical trial experience.
• Master’s degree in a relevant field preferred.
• Experience with HIPAA, FDA regulations, IRB requirements and Good Clinical Practices.
• Experience in clinical research, device development or pharmaceutical industry.
• Ability to establish priorities and manage multiple deadlines.
• Demonstrated ability to work independently and as part of a team.

Responsibilities

• Oversee subject recruitment and study enrollment goals.
• Oversee data management for research projects and ensure accurate reporting.
• Develop study schedules, targets, and accountabilities; lead team meetings.
• Supervise and mentor new staff or students; assist with evaluations.
• Audit operations for regulatory compliance and monitor IRB submissions.
• Collaborate with investigators and sponsors; monitor adverse events and resolve queries.
• Propose and implement improvements to policies and processes.

Skills

Investigator Initiated clinical trial

Master's degree preferred

HIPAA & FDA regulations experience

IRB requirements knowledge

Clinical research industry experience

Prioritization & deadline management

Independent and teamwork experience

Education

Bachelor’s degree in a related field

Master's degree preferred

Job description

Stanford Radiology in Palo Alto is seeking a Senior Clinical Research Coordinator (CRC2) to support multiple studies under the Investigator and Clinical Research Manager. You will develop recruitment strategies, oversee study operations, ensure regulatory compliance, and manage project progress.

The successful candidate will have strong communication and organizational skills, experience in clinical research, and the ability to handle shifting priorities while working with investigators,