Clinical Trial/Project Assistant #HRY

Job Scope Conduct pre-study, site initiation, routine monitoring and close-out visits in accordance with ICH-GCP, ClinActis SOPs and client requirements. Conduct site feasibility assessments and assist with investigator/site selection. 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 clinical trial sites. Review clinical trial protocols and Case Report Forms (CRFs) . Coordinate and present at Investigator Meetings . Participate in client meetings and bid defence meetings . Prepare and review Serious Adverse Event (SAE) reports . Prepare project/study status reports for clients and internal management. Manage study-related requests, queries and issues, including study supplies and third-party vendors . Verify completed CRFs and review clinical trial data. Resolve data queries with clinical trial site personnel. Review tables and listings generated from study data. Conduct on-site monitoring to oversee data collection, source documentation, CRFs and regulatory compliance . Ensure clinical trial sites are operating according to applicable regulations, protocols and quality standards Requirement Min 1 year clinical research experience 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)