Remote CRA for Global Phase II–IV Trials (Malaysia)

Planet Pharma; Malaysia; Remote; MYR 60,000 - 100,000; Full time

Benefits offered by this job

Leave entitlements

Health insurance

Retirement plans

Employee Assistance Programme (TELUS)

Job summary

Planet Pharma is hiring a Clinical Research Associate in Malaysia to oversee Phase II–IV trials with a focus on site initiation, monitoring, and close-out while ensuring compliance with ICH-GCP standards. The role requires strong data evaluation skills and excellent English communication.

The candidate should have at least 2 years of monitoring experience and a Bachelor’s degree in a related field. Travel up to 60% domestically and internationally is expected, with a remote-friendly work setup.

Qualifications

• Minimum of 2+ years monitoring experience in Phase I-III clinical trials.
• Bachelor’s degree in Medicine, Science, or an equivalent qualification.
• Proven experience in medium-sized study start-up and close-out procedures.
• Strong knowledge of ICH-GCP guidelines and medical data evaluation.
• Excellent written and verbal communication skills in English.
• Ability to travel at least 60% domestically and internationally; valid driver’s license required.

Responsibilities

• Independently set up, monitor, and close studies while maintaining comprehensive documentation and timely reports
• Submit protocols, consent forms, and regulatory documents for ethics and IRB approval
• Address sponsor queries effectively, ensuring seamless communication
• Monitor study costs to ensure budget adherence
• Prepare and review study documentation and conduct feasibility analyses for new proposals
• Potentially assist in training and mentoring fellow CRAs to uphold high standards across teams

Skills

Clinical monitoring

ICH-GCP knowledge

English proficiency

Travel willingness 60%+

Education

Bachelor’s degree in Medicine, Science, or related field

Tools

EDC systems

CTMS

Job description

Planet Pharma is hiring a Clinical Research Associate in Malaysia to oversee Phase II–IV trials with a focus on site initiation, monitoring, and close-out while ensuring compliance with ICH-GCP standards. The role requires strong data evaluation skills and excellent English communication.

The candidate should have at least 2 years of monitoring experience and a Bachelor’s degree in a related field. Travel up to 60% domestically and internationally is expected, with a remote-friendly work setup.