Clinical Trial Assistant (Perm, Office Hours) #HRY
Description
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.
Requirement
Degree in Pharmacy related discipline
Interested applicants, please email your updated CV to rachel.lim@recruitexpress.com.sg or WA 97527630 for more information.
We regret to inform that only shortlisted candidates will be contacted.
EA Personnel: Lim Ruo Yi, Rachel (R23116144)
Company EA license No.: Recruit Express Pte Ltd (99C4599)