Remote Clinical QA Specialist (GCP/Regulatory)

ManpowerGroup; Bethesda (MD); A distancia; USD 69.000 - 76.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Medical and Prescription Drug Plans

Dental Plan

Vision Plan

Health Savings Account

Health Flexible Spending Account

Dependent Care Flexible Spending App

Supplemental Life Insurance

Short Term and Long Term Disability

Business Travel Insurance

401(k) Plus Match

Weekly Pay

Descripción de la vacante

ManpowerGroup is seeking a Clinical Quality Assurance Specialist to join its QA team. You will support the Quality Management System and QA programs across clinical sites and vendors, ensuring regulatory compliance and continuous improvement.

The role emphasizes attention to detail, proactive problem solving, and strong communication in a dynamic environment. Remote work with flexible scheduling is available, with potential for growth within a leading clinical research organization.

Formación

• Knowledge of current GCP regulations and industry standards.
• Experience with regulatory agency audits and quality systems for CROs.
• Excellent written and verbal communication to document and convey information.
• Proficiency in MS Office applications to support daily tasks and documentation.
• Ability to work independently and collaboratively in a fast-paced environment.

Responsabilidades

• Support maintenance of the Quality Management System to ensure regulatory compliance.
• Maintain QA training, document control, customer complaint, and CAPA programs.
• Assist in audits of clinical sites and vendors to verify standards.
• Support internal audit programs and performance metrics for improvements.
• Manage review cycles of QA controlled documents to reflect procedures and audits.

Conocimientos

GCP regulations knowledge

Regulatory agency audits

Communication skills

Independent working

Team collaboration

Herramientas

MS Office

Descripción del empleo

ManpowerGroup is seeking a Clinical Quality Assurance Specialist to join its QA team. You will support the Quality Management System and QA programs across clinical sites and vendors, ensuring regulatory compliance and continuous improvement.

The role emphasizes attention to detail, proactive problem solving, and strong communication in a dynamic environment. Remote work with flexible scheduling is available, with potential for growth within a leading clinical research organization.