Clinical Trials Coordinator: Study Ops & Compliance

Sunway Medical Centre; Selangor; On-site; MYR 33,000 - 58,000; Full time

Job summary

Sunway Medical Centre's Sunway Clinical Research Centre is expanding its team to support investigators in planning and oversight of clinical trials. The role covers regulatory adherence, trial documentation, subject recruitment, and administration to ensure protocol compliance and data integrity.

The successful candidate will coordinate activities with sponsors, CRAs, and ethics committees, maintain study files, manage adverse events reporting, and assist with trial feasibility and close-out

Qualifications

• Degree in Nursing, Biomedical Sciences or Pharmacy; MBBS/MD also considered.
• Candidates with clinical pharmacy background preferred.
• At least 2 years in clinical research and trial.
• GCP Certification.

Responsibilities

• Assist investigator in clinical trial planning and ensure protocol/regulatory compliance.
• Coordinate subject recruitment, visits, and data collection per protocol.
• Maintain trial records, conduct AE/SAE reporting, and assist with CRF/eCRF entries.
• Liaise with sponsors, CROs, investigators, ethics committees and regulatory bodies.
• Plan training, monitor trial progress, and support trial close-out activities.

Skills

Microsoft Office

Excellent communication

Project management

Strategic thinking

Problem solving

Results driven

Adaptability

Education

Nursing degree

Biomedical Sciences degree

Pharmacy degree

MBBS/MD

Job description

Sunway Medical Centre's Sunway Clinical Research Centre is expanding its team to support investigators in planning and oversight of clinical trials. The role covers regulatory adherence, trial documentation, subject recruitment, and administration to ensure protocol compliance and data integrity.

The successful candidate will coordinate activities with sponsors, CRAs, and ethics committees, maintain study files, manage adverse events reporting, and assist with trial feasibility and close-out