Onsite Clinical Research Coordinator in La Jolla

knownwell; San Diego (CA); On-site; USD 65,000 - 90,000; Full time

Benefits offered by this job

Onsite Opportunity

Medical, dental, and vision insurance

401K retirement plan with company call

Up to 20 days of PTO per year + public

Up to 14 weeks of parental leave

Annual work from home stipend

Job summary

knownwell is hiring a Clinical Research Coordinator to oversee and coordinate all clinical trial activities in a primarily on-site La Jolla, San Diego setting. You will recruit, screen, and enroll patients, manage visits and data, and ensure regulatory compliance across trials.

The role requires phlebotomy skills, strong organizational abilities, and collaboration with investigators and sponsors. On-site work 4–5 days a week with comprehensive benefits is offered.

Qualifications

• Bachelor's degree in life sciences, nursing, or healthcare.
• CCRC Certification is preferred or willingness to obtain.
• Experience with FDA/ICH GCP guidelines is required.

Responsibilities

• Coordinate and manage all aspects of clinical trials, including patient recruitment, screening, and enrollment.
• Schedule and oversee patient visits, ensuring timely collection of data per protocol.
• Oversee site initiation, monitoring, closeout activities and equipment calibration for compliance.
• Maintain study documentation, including case report forms and consent forms.
• Review monitoring letters and resolve identified issues promptly.
• Ensure accurate reporting of adverse events and SAEs.
• Manage receipt, shipment, and storage of study drug and samples.
• Ensure proper handling and storage of study materials and biological samples.
• Generate invoices for study sponsors as applicable.

Skills

Phlebotomy

Study coordination

Regulatory compliance

Data management

Communication skills

Team collaboration

Education

Bachelor's degree in life sciences

CCRC Certification

Master’s degree preferred

Tools

CTMS

EDC

Regulatory software

Job description

knownwell is hiring a Clinical Research Coordinator to oversee and coordinate all clinical trial activities in a primarily on-site La Jolla, San Diego setting. You will recruit, screen, and enroll patients, manage visits and data, and ensure regulatory compliance across trials.

The role requires phlebotomy skills, strong organizational abilities, and collaboration with investigators and sponsors. On-site work 4–5 days a week with comprehensive benefits is offered.