Biotech CRA: Site Monitoring & Coordination

RECRUIT EXPRESS PTE LTD; Singapore; On-site; SGD 48,000 - 78,000; Full time

Job summary

RECRUIT EXPRESS PTE LTD in Singapore is seeking an experienced Clinical Research Monitor to oversee site activities in accordance with ICH-GCP and SOPs. You will conduct pre-study visits, site initiation, routine monitoring and data verification to ensure study quality.

The role involves coordinating with Principal Investigators and sites, negotiating budgets, reviewing CRFs and SAE reports, and preparing status updates for clients while maintaining regulatory compliance across sites.

Qualifications

• Min 1 year clinical research experience.
• Experience with ICH-GCP and SOPs.
• Ability to coordinate with investigators and sites.

Responsibilities

• Conduct pre-study, site initiation, routine monitoring and close-out visits per ICH-GCP and SOPs.
• Recruit and communicate with Principal Investigators (PIs) and investigator sites.
• Negotiate study budgets with investigators and institution representatives.
• Collect, review and process regulatory and administrative documents from trial sites.
• Review clinical trial protocols and CRFs; verify data and resolve data queries.
• Coordinate and present at Investigator Meetings and client meetings.

Skills

Clinical research

GCP compliance

Site monitoring

Budget negotiation

Regulatory documentation

Job description

RECRUIT EXPRESS PTE LTD in Singapore is seeking an experienced Clinical Research Monitor to oversee site activities in accordance with ICH-GCP and SOPs. You will conduct pre-study visits, site initiation, routine monitoring and data verification to ensure study quality.

The role involves coordinating with Principal Investigators and sites, negotiating budgets, reviewing CRFs and SAE reports, and preparing status updates for clients while maintaining regulatory compliance across sites.