Senior Clinical Research Associate I – Remote (NZ)

Health New Zealand - Te Whatu Ora Waitaha Canterbury

Christchurch

Remote

NZD 90,000 - 120,000

Full time

7 days ago
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Benefits offered by this job

Bonus eligibility
Total rewards package
Health & wellbeing benefits

Job summary

Thermo Fisher Scientific in Christchurch, NZ seeks a Senior Clinical Research Associate I to oversee monitoring and site management for clinical trials. This home-based role requires NZ residency with proximity to a major air hub.

The individual ensures protocol adherence, data integrity, and regulatory compliance while coordinating with CTMS and sponsors. The position emphasizes strong site management, timely communications, and collaboration with cross-functional teams to advance trials in

Qualifications

  • Bachelor's degree in life sciences or Registered Nursing certification.
  • NZ driver''s license required.
  • 4+ years of clinical research monitoring experience.

Responsibilities

  • Monitor investigator sites using a risk-based monitoring approach and ensure protocol compliance.
  • Conduct on-site and remote monitoring visits with data and documentation review.
  • Maintain study systems and CTMS updates; provide status reports to the Clinical Team Manager.
  • Participate in investigator meetings and site qualification activities as needed.
  • Ensure regulatory compliance and adherence to ICH-GCP throughout trials.

Skills

Clinical monitoring
ICH-GCP knowledge
Communication skills
Attention to detail
Time management
Teamwork

Education

Bachelor's degree life sciences or RN

Tools

Microsoft Office
CTMS

Job description

Thermo Fisher Scientific in Christchurch, NZ seeks a Senior Clinical Research Associate I to oversee monitoring and site management for clinical trials. This home-based role requires NZ residency with proximity to a major air hub.

The individual ensures protocol adherence, data integrity, and regulatory compliance while coordinating with CTMS and sponsors. The position emphasizes strong site management, timely communications, and collaboration with cross-functional teams to advance trials in

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