Clinical QA Specialist — Phase 1 Trials (Orlando Onsite)

Actalent; Orlando (FL); On-site; USD 26,000 - 34,000; Full time

Benefits offered by this job

Medical, dental & vision

401(k) Retirement Plan

Life Insurance

Short and long-term disability

Health Spending Account

Transportation benefits

Employee Assistance Program

PTO / Vacation

Job summary

Actalent is seeking a Quality Assurance Specialist for our Orlando, FL clinical research facility. The role focuses on reviewing clinical charts and ensuring quality in trials, with strong Microsoft Office usage for daily tasks in a fast-paced medical office environment.

The ideal candidate has an Associate's Degree, knowledge of QA methodologies, and experience in clinical research, including familiarity with IRB requirements.

Qualifications

• Proficiency in quality assurance and QA methodologies.
• Strong computer skills, particularly with Microsoft Office.
• Excellent communication skills.
• Experience in clinical research and familiarity with medical assistant duties.
• Knowledge of regulatory and Institutional Review Board requirements.

Responsibilities

• Review clinical charts to ensure quality standards are met for clinical trials.
• Perform data review and ensure compliance with regulatory requirements.
• Utilize Microsoft Office software to complete various office-related tasks.
• Maintain effective communication with team members and other stakeholders.
• Assist in healthcare-related tasks as needed within the scope of the role.

Skills

QA methodologies

Communication

Clinical research

IRB knowledge

Education

Associate's Degree

Tools

Microsoft Office

Job description

Actalent is seeking a Quality Assurance Specialist for our Orlando, FL clinical research facility. The role focuses on reviewing clinical charts and ensuring quality in trials, with strong Microsoft Office usage for daily tasks in a fast-paced medical office environment.

The ideal candidate has an Associate's Degree, knowledge of QA methodologies, and experience in clinical research, including familiarity with IRB requirements.