Contract Research Nurse – Pharma MNC | 2 Shifts, No Night Shift #HVN

Recruit Express Pte Ltd; Singapore; On-site; SGD 56,000 - 89,000; Full time

Benefits offered by this job

21 days annual leave

AWS (Annual Wage Supplement)

Job summary

Recruit Express Pte Ltd is hiring a Contract Research Nurse to support clinical trial activities for a leading pharmaceutical MNC. You'll work closely with investigators, study teams, and patients to ensure safe, accurate, and compliant conduct of studies.

Responsibilities include screening and coordinating study participants, assisting with informed consent and education, nursing assessments, ECGs, phlebotomy, and specimen collection, while ensuring drug accountability and study supply

Qualifications

• Valid nursing registration (e.g. SNB or equivalent).
• Diploma/Degree in Nursing required.
• Phlebotomy skills preferred.

Responsibilities

• Screen, recruit, and coordinate study participants.
• Support informed consent and patient education.
• Perform nursing assessments, vital signs, ECGs, phlebotomy, and specimen collection.
• Administer investigational products and monitor patients for reactions.
• Maintain source documentation and report adverse events.

Skills

Nursing

Phlebotomy

Communication skills

Education

Diploma/Degree in Nursing

Job description

Location: West

Job Type: Contract 1 year renewable, Training provided

Working Hours: 2 shifts only — no night shift

Benefits: 21 days annual leave, AWS (Annual Wage Supplement)

2 shifts only, no night shift

Opportunity to work with a Pharma MNC

Exposure to global clinical trials and research standards

About the Role

We are hiring a Contract Research Nurse to support clinicaltrial activities for a leading pharmaceutical MNC. You will work closely withinvestigators, study teams, and patients to ensure safe, accurate, andcompliant conduct of clinical studies.

Key Responsibilities:

• Screen, recruit, and coordinate studyparticipants
• Support informed consent process and patienteducation
• Perform nursing assessments, vital signs, ECGs,phlebotomy, and specimen collection
• Administer investigational products and monitorpatients for reactions
• Maintain accurate source documentation
• Report adverse events (AEs) and serious adverseevents (SAEs)
• Ensure drug accountability and study supplymanagement
• Comply with ICH-GCP, protocol, and regulatoryrequirements
• Coordinate study visits and communicate with thestudy team

Requirements

• Valid nursing registration (e.g. SNB orequivalent)
• Diploma/Degree in Nursing
• Experience in clinical research/clinical trialspreferred
• Phlebotomy skills preferred
• Meticulous, organised, and able to workindependently
• Good communication and interpersonal skills
• Able to commit to the contract duration