Hybrid Clinical Research Coordinator - Lead Studies, $40/hr

Avispa MedOps; Palo Alto (CA); Hybrid; USD 45,000 - 65,000; Part time

Benefits offered by this job

Group Medical

Dental

Vision

Life Insurance

Retirement Savings Program

PSL

Job summary

A leading university seeks a Clinical Research Coordinator to coordinate clinical studies from start-up through closeout, including participant enrollment, data management, and regulatory compliance. The role is hybrid in Palo Alto, CA, with a 40/hr wage and a 6-month assignment that may extend.

Responsibilities include coordinating studies, managing data, ensuring protocol compliance, and assisting with regulatory submissions and budget monitoring. Experience with EPIC and EMR is preferred.

Qualifications

• Coordinate clinical studies from start-up through closeout.
• Assist in regulatory submissions and IRB renewals.
• Experience with data collection, management, and regulatory compliance.

Responsibilities

• Coordinate moderately complex aspects of one or more clinical studies from start-up through closeout under close direction of the PI.
• Determine participant eligibility and obtain consent per protocol; assist in recruitment strategies.
• Collect and manage patient/lab data; maintain study databases and case report forms.
• Ensure compliance with protocols; audit CRFs; prepare regulatory submissions and monitor visits.
• Assemble study kits, monitor scheduling, and assist in budget adherence with finance.

Skills

Regulatory compliance

Recruitment coordination

Clinical data management

Microsoft Office

Sponsor/IRB liaison

Education

Associate degree in related field

Bachelor's degree in related field

Equivalent combination of education and experience

Tools

EPIC

Electronic Medical Records (EMR)

Job description

A leading university seeks a Clinical Research Coordinator to coordinate clinical studies from start-up through closeout, including participant enrollment, data management, and regulatory compliance. The role is hybrid in Palo Alto, CA, with a 40/hr wage and a 6-month assignment that may extend.

Responsibilities include coordinating studies, managing data, ensuring protocol compliance, and assisting with regulatory submissions and budget monitoring. Experience with EPIC and EMR is preferred.