Clinical Trial Study Coordinator: Hands-On Research & Patient Care

Prima Nexus Sdn Bhd; Kuala Lumpur; On-site; MYR 39,000 - 61,000; Full time

Job summary

Prima Nexus Sdn. Bhd. is seeking a responsible Clinical Trial Study Coordinator to support an ongoing clinical research project at Hospital Canselor Tuanku Muhriz (HCTM), Cheras.

The role provides hands-on exposure to real-world clinical research, including participant management, sample handling, and documentation. You will coordinate day-to-day activities, communicate with participants, and assist with on-site study visits, under supervision.

Qualifications

• Diploma/Degree in Biomedical Science or related Life Sciences.
• Basic laboratory and biological sample handling knowledge.
• Able to communicate confidently with study participants.
• Willingness to travel to HCTM Cheras and work on-site.

Responsibilities

• Coordinate day‑to‑day clinical study activities at HCTM.
• Manage and communicate with study participants.
• Coordinate participant appointments and study visits.
• Support participant screening and study documentation.
• Coordinate on‑site activities with investigators and research teams.
• Assist with biological sample collection.
• Perform sample processing including centrifugation and aliquoting.
• Ensure proper sample labelling, storage and tracking.
• Maintain accurate study records and logs.
• Follow study protocols, SOPs and research requirements.

Skills

Biological sample handling

Participant communication

Independent working

Organised and detail‑oriented

Interpersonal skills

Education

Diploma or Degree in Biomedical Science or related Life Sciences

Job description

Prima Nexus Sdn. Bhd. is seeking a responsible Clinical Trial Study Coordinator to support an ongoing clinical research project at Hospital Canselor Tuanku Muhriz (HCTM), Cheras.

The role provides hands-on exposure to real-world clinical research, including participant management, sample handling, and documentation. You will coordinate day-to-day activities, communicate with participants, and assist with on-site study visits, under supervision.