Senior CRA x2

Healthcare Professionals Group; Auckland; On-site; NZD 100,000 - 130,000; Full time

Job summary

A leading clinical research company in Auckland is seeking a Senior CRA to own and lead clinical activities across Phase I-III trials. In this role, you'll monitor various sites and build strong relationships with principal investigators and trial teams while contributing to study success and compliance. This position offers great autonomy and the opportunity to impact sponsor relationships significantly.

Qualifications

• 4 years’ independent monitoring experience, from site selection to close out.
• Phase II/III trial exposure.
• Ability to train, influence, and manage site staff.

Responsibilities

• Independently monitor sites across NZ for Phase I–III studies.
• Build strong site relationships with PIs, coordinators, and trial teams.
• Collaborate with project management, regulatory, and data teams.

Skills

Excellent communication skills

Site relationship management

Independent monitoring experience

Job description

Senior CRA – Lead Your Own Sites!

• Sponsor Facing with Full Site Ownership
• Early-Phase & Pivotal Trials
• Large Portfolio Across Multiple Therapeutic Areas

In this Senior CRA opportunity, you will step into an exciting new challenge owning your studies, lead clinical activity across phase I -III across multiple Therapeutic Areas, while being valued for your operational insight.

Our high-growth clinical research client is based in Auckland, renowned or its early-phase portfolio, strong site relationships, and empowering work culture.

The Opportunity:

• Independently monitor sites across NZ (SIVs, IMVs, COVs) for Phase I–III studies
• Build strong site relationships with PIs, coordinators, and trial teams
• Verify ICF, AE/SAE documentation, source data, and IMP accountability
• Collaborate with project management, regulatory, and data teams to drive trial timelines
• Identify and address site-level risks, deviations, and GCP compliance gaps
• Contribute to TMF accuracy, CAPAs, and regulatory submissions

Requirements:

• 4 years’ independent monitoring experience, from site selection to close out
• Phase II/III trial exposure
• Excellent communication skills with the ability to train, influence, and manage site staff

Salary & Package
$100,000 - $130,000 DOE (NZ Dollars)


If you're looking for autonomy, professional growth, and meaningful sponsor impact then please share your CV to Eve Cooke at [e-mail] or call me for a confidential conversation on [phone].