Associate Clinical Research Analyst - Tumor Institute

Providence Health & Services is a healthcare organization seeking an Associate Clinical Research Analyst to support research at its Tumor Institute. The role coordinates regulatory documentation and submissions for clinical research, supports human-subject protections, leads Research Assistants on a task basis, and provides training and workflow planning.

Responsibilities

• Prepares, facilitates, coordinates, and submits documentation required by federal, state and local regulations and institutional requirements relating to the conduct of research. This includes preparation of all submissions to the IRB to assure the protection of human subjects in research; FDA-required submissions which may include investigator 1572 forms, investigational new drug applications, device submissions such as Emergency use, HDE, Safety Reports, and other documents that may be required by a regulatory agency or the institution
• Leads the work of Research Assistants on a task-basis if applicable
• Provides on-the-job training, sets priorities and schedules workflow required to support project objectives

Benefits

• Additional compensation may be available for this role, such as shift differentials, standby/on-call, overtime, premiums, extra shift incentives, or bonus opportunities.
• A retirement 401(k) Savings Plan with employer matching
• Health care benefits (medical, dental, vision)
• Life insurance
• Disability insurance
• Paid parental leave
• Vacations
• Holidays
• Time off for health issues
• Voluntary benefits
• Well-being resources

Company

• Healthcare provider operating hospitals, clinics, and social services
• Renton, Washington, USA
• https://www.providence.org/
• Founded in 1859
• 10001+ employees

Qualifications

• Bachelor's degree preferably in science, healthcare, pharmacy, or other related field, or significant experience in research coordination or regulatory work may be substituted for educational requirements
• 2 years of experience in healthcare, research or clinical setting with regulatory compliance familiarity

Required skills

• Clinical Research, Regulatory Compliance, Research Coordination

Experience

• 2+ years