Key Responsibilities:

• • Perform QA review of participant files, source documents, and CRFs.
• • Conduct QC checks for completeness, accuracy, and protocol compliance.
• • Identify quality issues, deviations, and documentation gaps.
• • Assist in CAPA development and tracking.
• • Prepare QA/QC reports and support monitoring visits and audits.
• • Coordinate with study team to ensure compliance with SOPs and regulations.

Must have:

• • Bachelor of Science degree.
• • With 1-3 years of clinical research experience.
• • Preferably with TB or HIV research experience.
• • Knowledge of ICH-GCP and regulatory requirements.
• • Strong attention to detail and documentation accuracy.
• • Profecient in Microsoft Office applications
• • Able to work independently and collaboratively

Your Role:

• • Conduct clinical assessments and manage study participants according to protocol.
• • Ensure adherence to ethical and regulatory requirements.
• • Collaborate with research staff and investigators for smooth project implementation.
• • Prepare and review clinical documentation and reports.

Must have:

• • Medical degree and valid PRC license.
• • Experience in clinical research or hospital practice preferred.
• • Knowledge of Good Clinical Practice (GCP) guidelines.
• • Strong analytical, communication, and decision-making skills.