Singapore | Posted: Jul 15, 2026

Main Purpose:
Support Clinical Project Managers (CPMs) and study team with administrative, documentation, TMF, budget management and logistic activities related to Clinical studies during the operational phase of clinical trials to ensure the timely delivery of quality data while complying with internal Standard Operating Procedures, applicable laws and ICH Good Clinical Practice.

-Supports maintenance of clinical studies management tracking tools and trackers. Support study team to register study on ct.gov.
-Assists study team with trial management logistical support (sample or ancillary shipments, procurement of study supplies, organizing trainings).
-Assists study team in the quality check of protocols, informed consent forms and advertisement materials to ensure compliance with SOPs and regulatory requirements.
-Supports organization of clinical meetings (internal meetings, meetings with CROs, Investigators meetings, etc.) including agenda, minutes, logistics.
-Assists in managing global communications (e.g., Newsletters, emails, website posting).
-Assists with the preparation, review and maintenance of SOPs, work instructions, training materials, and templates related to project activities.
-Contributes to continuous improvement of working processes (for example supporting data entry into CTMS, SOP/SWI revision)

Interested candidates submit your resume to:
TELE: @klrqi
WA: https://wa.me/+6598328891
Email: medical12@recruitexpress.com.sg

Jace Choo Oi Kei
Personnel EA License No.: R1875164
Recruit Express Pte Ltd (EA Licence No.: 99C4599)