Responsibilities

·       Coordinate and support clinical research studies and trials.

·       Screen and recruit suitable participants according to study protocols.

·       Collect, enter, and maintain accurate study data and documentation.

·       Schedule study visits and liaise with investigators, patients, and stakeholders.

·       Ensure compliance with study protocols, regulatory requirements, and Good Clinical Practice (GCP) guidelines.

·       Prepare reports and assist with ethics submissions and study-related administration.

·       Manage research databases and maintain study records.

Requirements

·       Degree in Life Sciences, Biomedical Science, Nursing, Pharmacy, Public Health, or related discipline.

·       Prior experience in clinical research or healthcare setting preferred.

·       Familiarity with GCP guidelines is an advantage.

·       Strong organizational and coordination skills.

·       Meticulous, detail-oriented, and able to manage multiple projects simultaneously.

·       Good communication and interpersonal skills.

·       Benefits

Interested candidates please send in your resume to:

nurse@recruitexpress.com.sg

Anthea Lim

Outsourcing Team

Recruit Express Pte Ltd, EA License No.: 99C4599