Clinical Trial Assistant (Perm, Office Hours) #HRY

Your tasks

Job Scope

• Conduct pre-study, site initiation, routine monitoring and close-out visits in compliance with ICH-GCP, SOPs and regulatory requirements.
• Perform site feasibility assessments and support investigator/site selection and recruitment.
• Liaise with Principal Investigators (PIs), clinical trial sites, clients and institutional representatives.
• Negotiate study budgets and coordinate investigator meetings, client meetings and bid defence presentations.
• Collect, review and process regulatory, administrative and clinical trial documents.
• Review study protocols, Case Report Forms (CRFs) and clinical trial data to ensure accuracy and completeness.
• Monitor clinical trial sites to ensure proper data collection, source documentation and regulatory compliance.
• Prepare Serious Adverse Event (SAE) reports and study status reports.
• Manage study-related queries, issues, supplies and vendors, ensuring timely resolution of data discrepancies.

Requirements

Degree in Pharmacy related discipline

How to apply

Interested applicants, please email your updated CV to rachel.lim@recruitexpress.com.sg or WA 97527630 for more information.

Other

EA Personnel: Lim Ruo Yi, Rachel (R23116144)