Cardiac Clinical Research Coordinator — Impactful Trials

National University Health System

Singapore

Sur place

SGD 52 000 - 76 000

Plein temps

14 jours+

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Résumé du poste

National University Health System in Singapore seeks a dedicated healthcare professional to assist investigators in clinical trials. You will support screening, recruitment, informed consent, venepuncture, specimen handling, and data entry per GCP and HBRA requirements.

Role requires a nursing or life science background with clinical research experience, strong communication, meticulousness, and teamwork. On-site work in a hospital setting with adherence to study protocols and regulatory

Qualifications

  • Degree in Nursing or Life Science/Healthcare related courses or Diploma with clinical research experience.
  • Previous work experience in clinical research or nursing is advantageous.
  • Good written and verbal communication; multilingual abilities are a plus.
  • Able to work meticulously, independently and as part of a team.

Responsabilités

  • Assist investigators in screening, recruitment, and follow-up visits of potential patients.
  • Assist investigators in obtaining informed consent.
  • Perform venepuncture and cannulation as required by protocol.
  • Schedule appointments for patients/subjects and maintain trial records.
  • Dispense study drugs and perform drug reconstitution under supervision.
  • Coordinate trial study activities, complete CRFs, and ensure data accuracy.
  • Assist with ethics submissions and regulatory documentation as required.

Connaissances

Nursing knowledge
Clinical research experience
Interpersonal skills
Communication skills
Attention to detail
Team player

Formation

Bachelor or Diploma in Nursing/Life Science/Healthcare
Relevant clinical research experience

Description du poste

National University Health System in Singapore seeks a dedicated healthcare professional to assist investigators in clinical trials. You will support screening, recruitment, informed consent, venepuncture, specimen handling, and data entry per GCP and HBRA requirements.

Role requires a nursing or life science background with clinical research experience, strong communication, meticulousness, and teamwork. On-site work in a hospital setting with adherence to study protocols and regulatory

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