Clinical Trials Project Coordinator

RECRUIT EXPRESS PTE LTD; Singapore; On-site; SGD 42,000 - 58,000; Full time

Job summary

RECRUIT EXPRESS PTE LTD in Singapore is seeking a proactive Clinical Project Support professional to assist the project manager and clinical team. The role focuses on maintaining study and site documentation, tracking CRFs, and supporting regulatory submissions within project timelines.

The ideal candidate has prior experience in clinical trials and documentation, and will support administrative and data flow tasks across the project lifecycle in a fast-paced environment.

Qualifications

• Prior experience assisting in clinical trial and documentation

Responsibilities

• Update and maintain clinical systems that track study and site compliance and performance within project timelines.
• Assist with preparation, handling, distribution, filing, and archiving of clinical documentation and reports.
• Assist with periodic review of study files for accuracy and completeness and to support with project-related filing.
• Assist with the tracking and management of Case Report Forms (CRFs), queries, and clinical data flow.
• Assist in handling project-related administrative matters, such as preparation for regulatory submissions, safety report handling, and other logistic issues.
• Assist with Project finance related activities including project expenses invoice preparation and tracking as well as site payment invoice review, preparation and tracking.
• Act as a central contact for the clinical team for designated project communications, correspondence, and associated documentation including communication with sponsor and vendors as delegated.
• Support any other project related tasks as assigned.

Job description

RECRUIT EXPRESS PTE LTD in Singapore is seeking a proactive Clinical Project Support professional to assist the project manager and clinical team. The role focuses on maintaining study and site documentation, tracking CRFs, and supporting regulatory submissions within project timelines.

The ideal candidate has prior experience in clinical trials and documentation, and will support administrative and data flow tasks across the project lifecycle in a fast-paced environment.