Remote GCP QA Specialist - Clinical Trials

Placements24; Mbombela (Nelspruit); Hybrid; ZAR 550,000 - 850,000; Full time

Benefits offered by this job

Competitive salary

Health benefits

Retirement savings plan

Online training

Virtual workshops

Job summary

Placements24 is seeking a meticulous Remote Quality Assurance Specialist to ensure GCP compliance across clinical trial operations. This fully remote role allows you to contribute to research integrity from home in South Africa.

You will conduct internal audits, review trial documentation, and support QMS development while staying current with GCP guidelines and regulatory expectations.

Qualifications

• Bachelor-level degree in a scientific or healthcare field is required.
• At least 4 years in Quality Assurance or Clinical Research with GCP focus.
• Strong knowledge of GCP guidelines (ICH, FDA, EMA) and practical use.
• Experience in audits, documentation review and reporting.
• Excellent written/verbal communication and remote work discipline.

Responsibilities

• Conduct internal audits of trial documentation and systems for GCP compliance.
• Review protocols, informed consent forms and investigator site files.
• Monitor adherence to study procedures and regulatory requirements.
• Identify compliance issues and propose corrective actions.
• Assist in developing and maintaining Quality Management Systems (QMS).
• Support external audits and inspections by regulators.
• Help train clinical research staff on GCP principles and compliance.
• Prepare audit reports with findings and follow-up actions.
• Stay updated on evolving GCP regulations and best practices.
• Participate in quality improvement initiatives and process enhancements.

Skills

GCP knowledge

Audits

Clinical Research

Documentation

MS Office

Remote work

Education

Bachelor's degree in a relevant scientific or healthcare field

Job description

Placements24 is seeking a meticulous Remote Quality Assurance Specialist to ensure GCP compliance across clinical trial operations. This fully remote role allows you to contribute to research integrity from home in South Africa.

You will conduct internal audits, review trial documentation, and support QMS development while staying current with GCP guidelines and regulatory expectations.