Clinical Research Associate — Monitoring & Compliance

Expecto Health Science; Kuala Lumpur; Híbrido; MYR 60.000 - 120.000; Jornada completa

Descripción de la vacante

Expecto Health Science in Malaysia is seeking a Clinical Monitoring professional to perform on-site and remote monitoring, ensuring adherence to the study protocol, regulations, and GCP requirements.

The role involves reviewing CRFs and source documents, documenting deviations, communicating with investigators and sponsors, and supporting site initiation, routine monitoring, and close-out activities while keeping meticulous trial records.

Formación

• Ability to communicate effectively with investigators and teams.
• Strong organizational and time-management abilities.
• Good problem-solving and analytical skills.
• Excellent attention to detail and accuracy.
• Willingness to travel to trial sites as required.

Responsabilidades

• Conduct on-site and remote monitoring visits to ensure GCP and protocol compliance.
• Review CRFs and source documents for data accuracy and completeness.
• Identify and follow up on protocol deviations and data discrepancies.
• Communicate with investigators, site staff, sponsors, and teams to support progress.
• Prepare monitoring visit reports and close action items on time.
• Support site initiation, routine monitoring, and close-out activities.
• Maintain trial documentation and aid inspection readiness.

Conocimientos

Communication skills

Organizational skills

Problem-solving

Attention to detail

Multitasking

Travel willingness

Educación

Degree in Life Sciences / Pharmacy / Nursing / Medicine

Descripción del empleo

Expecto Health Science in Malaysia is seeking a Clinical Monitoring professional to perform on-site and remote monitoring, ensuring adherence to the study protocol, regulations, and GCP requirements.

The role involves reviewing CRFs and source documents, documenting deviations, communicating with investigators and sponsors, and supporting site initiation, routine monitoring, and close-out activities while keeping meticulous trial records.