Clinical Trial Manager

i-Pharm Consulting; Auckland; Presencial; NZD 90 000 - 120 000; Tempo integral

Resumo da oferta

i-Pharm Consulting in New Zealand seeks an experienced Clinical Trial Manager to own delivery from study award through close-out. You will partner with sponsors and CROs to drive performance, timelines and budgets in a collaborative, quality-driven environment.

This permanent, full-time role offers significant scope to shape study strategy and contribute to impactful therapies. Ideal candidates have around five years in clinical research, with proven trial/program management, strong stakeholder

Qualificações

• Around 5 years' experience within clinical research.
• Experience managing clinical trials, projects or programmes.
• Strong sponsor, CRO and stakeholder management skills.
• Good understanding of ICH-GCP and regulatory requirements.
• Experience overseeing study budgets, timelines and delivery.

Responsabilidades

• End-to-end ownership of clinical trial delivery from study award through to close-out.
• Act as the key operational contact for sponsors, CROs and external partners.
• Influence study strategy, timelines, budgets and operational performance.
• Work within a collaborative, quality-driven research environment.
• Contribute to studies that help bring new treatments and therapies to patients.

Conhecimentos

Sponsor management

Stakeholder management

ICH-GCP knowledge

Budget management

Trial delivery ownership

Descrição da oferta de emprego

Clinical Trial Manager | New Zealand | Permanent, Full-Time

An exciting opportunity for an experienced clinical research professional to step into a newly created Clinical Trial Manager position with a highly regarded research organisation.

This is an opportunity to take real ownership of clinical trial delivery, work closely with sponsors and CROs, and play a key role in the continued growth of the organisation.

What makes this opportunity interesting?

• Newly created position with scope to make an impact.
• End-to-end ownership of clinical trial delivery, from study award through to close-out.
• Act as the key operational contact for sponsors, CROs and external partners.
• Influence study strategy, timelines, budgets and operational performance.
• Work within a collaborative, quality-driven research environment.
• Contribute to studies that help bring new treatments and therapies to patients.

What we're looking for:

• Around 5 years' experience within clinical research.
• Experience managing clinical trials, projects or programmes.
• Strong sponsor, CRO and stakeholder management skills.
• Good understanding of ICH-GCP and regulatory requirements.
• Experience overseeing study budgets, timelines and delivery.