Global Research Compliance Coordinator

University of California, San Francisco; San Francisco (CA); On-site; USD 90,000 - 120,000; Full time

Job summary

University of California, San Francisco is seeking a Research Compliance Analyst 2 (Study Administrator) to support oversight of research protocols, HIPAA and IRB processes, and regulatory compliance across multiple sites. You will help prepare protocols, obtain approvals, and assist with data collection and manuscript preparation.

The role includes monitoring protocol adherence, coordinating with study personnel, and contributing to grant and manuscript writing, with opportunities for site

Qualifications

• Bachelor's degree in related area and / or equivalent experience / training.
• 2 years experience in administrative analysis or operations research or an equivalent combination of education and experience
• 1-2 years' experience with study coordination
• Experience with statistical software packages (R or STATA)
• Understanding of HIPAA and IRB approval process
• Experience in writing, editing, and reviewing scientific manuscripts

Responsibilities

• Staff, administer or manage research oversight and compliance committee activities.
• Assist in preparing for study implementation, including refining study protocols and obtaining regulatory approvals.
• Monitor adherence to study protocol across sites and prepare monitoring reports for NIH and Data Safety Monitoring Committees.
• Assist with grant and manuscript writing, data management and analysis, including data cleaning and form design.

Skills

Strong writing

Communication skills

Teamwork

Analytical thinking

R programming

Education

Bachelor's degree or equivalent experience

Graduate degree in public health/nursing/epidemiology or related field

Tools

R

STATA

Job description

University of California, San Francisco is seeking a Research Compliance Analyst 2 (Study Administrator) to support oversight of research protocols, HIPAA and IRB processes, and regulatory compliance across multiple sites. You will help prepare protocols, obtain approvals, and assist with data collection and manuscript preparation.

The role includes monitoring protocol adherence, coordinating with study personnel, and contributing to grant and manuscript writing, with opportunities for site