Neurosurgery Research Coordinator: Neuromodulation

National University Hospital; Singapore; On-site; SGD 42,000 - 66,000; Full time

Job summary

National University Hospital is seeking a Clinical Research Coordinator to support neuromodulation studies, including transcranial magnetic stimulation, vagal nerve stimulation, and deep brain stimulation, in patients with neurological and neuropsychiatric diseases.

The role involves coordinating ethics applications, participant recruitment, data collection, consent, and study logistics in a hospital setting, with HBRA/GCP guidelines.

Qualifications

• Fast learner who can take initiative and solve problems.
• Able to work independently and as part of a team.
• Demonstrates leadership, accountability and ownership of tasks.
• Excellent interpersonal and organizational skills.
• Able to manage multiple projects and work under pressure in a fast-paced environment.
• Good written and verbal communication skills.
• Proficiency or familiarity with Mandarin, Malay, Tamil or Chinese dialects is an added advantage.

Responsibilities

• Coordinate ethics applications, grant management, site initiation, recruitment, data collection, and study close-out.
• Identify, recruit, and screen potential subjects based on protocol criteria.
• Administer informed consent to enrolled subjects.
• Schedule visits/procedures and send reminders to ensure retention.
• Ensure proper collection, management and storage of research data and biological samples.
• Maintain investigator files and logs, including consent records and blood collection.

Skills

Fast learner

Independent

Team player

Leadership

Interpersonal skills

Project management

Written communication

Multilingual advantage

Education

Diploma/degree in Science, Life Sciences, or Nursing

Job description

National University Hospital is seeking a Clinical Research Coordinator to support neuromodulation studies, including transcranial magnetic stimulation, vagal nerve stimulation, and deep brain stimulation, in patients with neurological and neuropsychiatric diseases.

The role involves coordinating ethics applications, participant recruitment, data collection, consent, and study logistics in a hospital setting, with HBRA/GCP guidelines.