Clinical Site Manager | Clinical Operations Manager | Auckland
CSM_CSM20112024
Posted: 20/11/2024
- NZD130000 - NZD150000 NZD130000.00-NZD150000.00
- Auckland, New Zealand
- Permanent
An opportunity to join a leading Clinical Trial Site Network in Auckland, New Zealand as the Site Manager.
This company have been hugely successful over recent years and are continuing to grow. They have conducted hundreds of clinical trials across a range of therapeutic areas and phases, and so are truly specialist in the work they produce – covering early and late phase.
They have a committed team onsite, working in a collaborative approach, and are looking for someone to join who shares these values and can lead the unit.
Being a growing company means more room for career progression too, with the ability to upskill in a range of project scope.
This role would suit an experienced Clinical Site Manager / Clinical Operations manager at site level. Candidates must have extensive clinical trial experience.
About Them
This organisation is a premier clinical trial site network operating across New Zealand and Australia, with over 20 years of experience in conducting cutting-edge clinical research. Their network includes 10+ fully integrated clinical trial sites, making them one of the largest in Australasia.
The Role
As our Clinical Site Manager, you will be responsible for overseeing the day-to-day operations of one of our key clinical trial sites in New Zealand. You'll manage a diverse portfolio of studies ranging from early phase to phase IV trials across various therapeutic areas.
Title: Clinical Site Manager
Location: Auckland
Salary: $130,000 - $150,000NZD
Key Responsibilities
- Lead and mentor a team of clinical research coordinators and support staff
- Ensure compliance with Good Clinical Practice (GCP), regulatory requirements, and internal SOPs
- Oversee patient recruitment, screening, and retention strategies
- Manage site budgets and resource allocation
- Liaise with sponsors, CROs, and regulatory bodies
- Implement quality control measures to maintain high data integrity
- Contribute to business development initiatives and site growth strategies
Qualifications and Experience
- Bachelor's degree in a health-related field; advanced degree preferred
- Minimum 5 years of experience in clinical research, with at least 2 years in a management role
- In-depth knowledge of ICH-GCP guidelines and regulatory requirements
- Strong leadership and interpersonal skills
- Experience with a wide range of therapeutic areas and study phases
Keeley Munday
Principal Candidate Consultant
