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

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

recruit express pte ltd
3-6 Years
SGD 3,000 - 4,000 per month
  • Posted 18 hours ago
  • Be among the first 10 applicants

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

Interested candidates please send in your resume to:

[Confidential Information]

Anthea Lim

Outsourcing Team

Recruit Express Pte Ltd, EA License No.: 99C4599

More Info

Job Type:
Industry:
Employment Type:

Key Skills

Nursing assessments

ECGs

Source documentation

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Report adverse events (AEs) and serious adverse events (SAEs), specimen collection , Nursing assessments, Drug accountability, Study supply management, Phlebotomy, Administer investigational products, Clinical research, Clinical Trials, ECGs