Clinical Research Analyst

This is a fully remote position, open to applicants in California, +2 more states.

📋 Description

• Conduct comprehensive full-board and expedited reviews.

• Manage adverse events, protocol changes, informed consent documents, and other research-related activities.

• Evaluate and review regulatory submissions and actions pertaining to human subjects research for IRB evaluation.

• Offer support to IRB members as needed.

• Act as a resource for individuals engaging in research within the health system.

• Facilitate communication between the IRB and researchers.

• Ensure adherence to regulatory and institutional standards.

⛳️ Requirements

• Minimum of 4 years of experience in a health-related field or research, or a comparable combination of education and experience.

• At least 3 years of experience in IRB, regulatory, or research roles.

• Preferred: 4 years of experience in IRB, regulatory, or research settings.

• Preferred: 2 years of experience utilizing an electronic IRB platform.

• CIP Certification is preferred.

🏝️ Benefits

• Retirement 401(k) Savings Plan with employer matching.

• Comprehensive health care benefits (medical, dental, vision).

• Life insurance coverage.

• Disability insurance options.

• Paid parental leave.

• Vacation and holiday time off.

• Time off for health-related issues.

• Voluntary benefits available.

• Well-being resources for employees.

• An inclusive workplace that values diversity.

• Additional compensation opportunities may include shift differentials, standby/on-call pay, overtime, premiums, extra shift incentives, or bonuses.