Clinical Research Coordinator Nurse – (East) #HVY

Recruit Express Pte Ltd; Singapore; In loco; SGD 60.000 - 85.000; Tempo pieno

Descrizione del lavoro

Recruit Express Pte Ltd is seeking a Registered Nurse to join a research team as a Clinical Research Coordinator Nurse in the East. You will support clinical trials, ensure patient safety and protocol adherence, and collect high-quality data.

Responsibilities include coordinating visits, recruiting participants, obtaining informed consent, administering study meds where applicable, and reporting adverse events while liaising with investigators, sponsors, and regulators.

Competenze

• Valid nursing registration (e.g. SNB).
• Diploma or Degree in Nursing.
• GCP certification is an advantage.
• Experience in clinical research/clinical trials preferred.

Mansioni

• Coordinate and conduct clinical study visits.
• Screen, recruit, and follow up with study participants.
• Support the informed consent process and patient education.
• Administer study medication or investigational products where applicable.
• Report adverse events (AEs) and serious adverse events (SAEs).
• Liaise with Principal Investigators, study teams, sponsors, and ethics/regulatory bodies.
• Manage study supplies and drug accountability.
• Ensure compliance with ICH-GCP, protocol, and hospital guidelines.

Formazione

Diploma or Degree in Nursing

Strumenti

Phlebotomy

ECG

Descrizione del lavoro

Location: East Side

Job Type: [Full-Time / Contract / Renewable]

Working Hours: [ Office hours / 5-day work week]

About the Role

We are looking for a registered nurse to join a research team in the East as a Clinical Research Coordinator Nurse.

You will support clinical trials and research studies, ensuring patient safety, protocol compliance, and high-quality data collection.

Key Responsibilities

• Coordinate and conduct clinical study visits
• Screen, recruit, and follow up with study participants
• Support the informed consent process and patient education
• Administer study medication or investigational products where applicable
• Report adverse events (AEs) and serious adverse events (SAEs)
• Liaise with Principal Investigators, study teams, sponsors, and ethics/regulatory bodies
• Manage study supplies and drug accountability
• Ensure compliance with ICH-GCP, protocol, and hospital guidelines

Requirements

• Valid nursing registration (e.g. SNB)
• Diploma or Degree in Nursing
• Experience in clinical research/clinical trials preferred
• GCP certification is an advantage
• Phlebotomy and ECG skills preferred
• Meticulous, organized, and able to work independently
• Good communication and interpersonal skills