Clinical Research Associate (Training Provided) #HTJ

RECRUIT EXPRESS PTE LTD; Singapore; On-site; SGD 36,000 - 43,000; Full time

Job summary

Recruit Express Pte Ltd in Singapore is seeking a detail‑oriented project support professional to assist the Clinical Team with day‑to‑day activities and to help keep study files up to date. You will maintain clinical systems, handle regulatory submissions, and coordinate communications with sponsors, vendors, and sites, ensuring timelines are met and data quality is upheld.

Applicants should hold a science-related bachelor's degree; internship experience in clinical research or healthcare is

Qualifications

• Bachelor's Degree in a science-related discipline.
• Internship experience in clinical research, laboratories, healthcare, or related field is welcome.

Responsibilities

• Support the Project Manager and Clinical Team with day-to-day project activities.
• Update and maintain clinical systems to track study and site compliance within project timelines.
• Prepare, distribute, file, and archive clinical documents and study reports.
• Review study files to ensure accuracy and completeness.
• Track and manage Case Report Forms (CRFs), clinical queries, and data flow.
• Assist with regulatory submissions, safety reports, and other project administrative tasks.
• Support project finance activities, including expense and invoice tracking, as well as site payment reviews.
• Coordinate project communications with sponsors, vendors, and internal stakeholders.
• Provide additional project support as assigned.

Education

Bachelor's Degree in a Science-related discipline

Job description

Location: Central

Salary: Up to S$3,500

Working Hours: Monday to Friday, Office Hours

Job Scope

• Support the Project Manager and Clinical Team with day-to-day project activities.
• Update and maintain clinical systems to track study and site compliance within project timelines.
• Prepare, distribute, file, and archive clinical documents and study reports.
• Review study files to ensure accuracy and completeness.
• Track and manage Case Report Forms (CRFs), clinical queries, and data flow.
• Assist with regulatory submissions, safety reports, and other project administrative tasks.
• Support project finance activities, including expense and invoice tracking, as well as site payment reviews.
• Coordinate project communications with sponsors, vendors, and internal stakeholders.
• Provide additional project support as assigned.

Requirements

• Bachelor's Degree in a Science-related discipline.
• Internship experience in clinical research, laboratories, healthcare, or a related field is welcome.