Research Assitant

$41,600 - $47,840/Yr

Dr. Kay Durairaj - BeautyByDrKay - Pasadena, CA

Full-time

Pasadena, CA

About the position

The Research Associate position is a full-time role focused on coordinating clinical research studies within a private practice specializing in aesthetic clinical studies. The role involves working closely with potential patients and ensuring compliance with study protocols and regulatory requirements.

Responsibilities

• Assist with IRB approval.
• Organize and schedule assessments/tests/activities to meet research objectives and study protocol compliance.
• Oversee the data collection and management of the data for the project.
• Communicate with study team personnel to ensure study procedures are followed and research is performed as described in the protocol.
• Serve as contact for subjects, study personnel, Institutional Review Board (IRB), and study sponsor.
• Develop or assist with the development of study design, protocols, and other study-specific documents essential for the appropriate implementation of clinical investigation.
• Work with investigators to ensure optimal compliance and performance to the protocol, regulatory requirements, discrepancy reporting, and ethical practice.
• Assist with the submission of timely, accurate, and complete study continuing review, amendments, and reportable events to IRB.

Requirements

• Bachelor's degree or equivalent work experience with clinical research knowledge.
• Previous experience working in either an academic or commercial clinical trials environment.
• Knowledge of FDA and other regulatory agency rules and regulations.
• Ability to create and manage a budget.
• Ability to work without supervision.
• Effectively interview and select candidates.
• Ability to produce and present clear, concise, and professionally written communications and presentations.
• Performance management, effective coaching, and directing of others.
• Positive attitude and motivation.
• Visionary and forward-thinking.
• Project management skills.
• Strong PC skills, including MS Outlook, Word, etc.
• Strong critical thinking and decision-making skills.

Nice-to-haves

• Experience in clinical trials (1 year required).
• Experience in research (1 year required).

Benefits

• Employee discount