Clinical Research Nurse - Phase 1 Trials, 24/7 Roster

Nucleus Network

St Leonards

On-site

AUD 70,000 - 100,000

Full time

4 days ago
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Benefits offered by this job

Fitness Passport
Reward Hub discounts
Wellbeing initiatives
EAP support

Job summary

Nucleus Network in NSW is seeking a Clinical Research Nurse to support early-phase trials, providing high-quality patient care and accurate data collection while working across a 24/7 rotating roster. Full training will be provided and you will collaborate with a multidisciplinary team.

You will conduct assessments, administer Investigational Products and medications, monitor participants, and ensure compliance with ICH-GCP guidelines.

Qualifications

  • Registered Division 1 Nurse with AHPRA (NSW) in good standing.
  • Minimum 2 years post-graduate experience in an acute care setting.
  • Ability to work in a fast-paced environment and manage time effectively.
  • Excellent communication with participants and health care professionals.

Responsibilities

  • Assisting in the coordination and supervision of staff and participants within the clinical unit
  • Ensuring procedures and guidelines are conducted to industry standards
  • Administering Investigational Products, prescription and medications
  • Providing general nursing care, monitoring patient’s well-being and taking appropriate action when necessary
  • Conduct procedures such as vital signs, ECGs, blood collection, blood processing and data collection
  • When required, acting as the nurse in charge and working within a higher scope of practice

Skills

Time management
Communication
Interpersonal skills
Clinical nursing

Education

Registered Division 1 Nurse with AHPRA

Job description

Nucleus Network in NSW is seeking a Clinical Research Nurse to support early-phase trials, providing high-quality patient care and accurate data collection while working across a 24/7 rotating roster. Full training will be provided and you will collaborate with a multidisciplinary team.

You will conduct assessments, administer Investigational Products and medications, monitor participants, and ensure compliance with ICH-GCP guidelines.

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