Clinical Project Manager

i-Pharm Consulting; Sydney; On-site; AUD 120,000 - 180,000; Full time

Job summary

i-Pharm Consulting is seeking an experienced Clinical Project Manager for a Sydney-based site focusing on healthy volunteer Phase I studies. The role emphasizes collaboration with sponsors and internal teams to drive trials from initiation to completion.

You will oversee end-to-end trial delivery, manage timelines and budgets, and act as a primary liaison with stakeholders while ensuring adherence to GCP and regulatory standards.

Qualifications

• Experience as Clinical Project Manager in a trial site, CRO or early-phase research environment.
• Strong knowledge of clinical trial processes and GCP.
• Excellent stakeholder management and communication skills.
• Natural ability to bring people together and drive alignment.

Responsibilities

• Oversee end-to-end delivery of healthy volunteer trials.
• Manage study timelines, budgets, milestones and deliverables.
• Act as the key contact for sponsors and external stakeholders.
• Work closely with clinical operations, investigators and site teams.
• Proactively identify challenges and keep studies on track.
• Ensure studies are delivered in accordance with GCP, protocols and regulatory requirements.
• Build strong relationships across the business to drive trial outcomes.

Skills

Stakeholder management

Communication skills

Leadership

Problem solving

Job description

Sydney | City Fringe | Clinical Trial Site

Love clinical trials? Know your way around Phase I studies? This could be right up your alley!

I'm partnering with an established clinical trial site on the Sydney city fringe that's looking to welcome an experienced Clinical Project Manager to their team.

This is a fantastic opportunity for someone who enjoys being close to the action, working collaboratively with sponsors and internal teams, and seeing clinical trials come to life from start to finish.

We're keen to speak with Project Managers who have a passion for early-phase research and enjoy the variety that comes with delivering healthy volunteer studies.

What you'll be doing

• Overseeing the end-to-end delivery of healthy volunteer clinical trials
• Managing study timelines, budgets, milestones and deliverables
• Acting as a key point of contact for sponsors and external stakeholders
• Working closely with clinical operations, investigators and site teams
• Proactively identifying challenges and keeping studies on track
• Ensuring studies are delivered in accordance with GCP, protocols and regulatory requirements
• Building strong relationships across the business and contributing to successful study outcomes

What we're looking for

• Previous Clinical Project Management experience within a clinical trial site, CRO or early-phase research environment
• Strong knowledge of clinical trial processes and GCP requirementsExcellent stakeholder management and communication skills
• A natural ability to bring people together and keep everyone moving in the same direction
• Someone who enjoys taking ownership, finding solutions and making things happen

Why consider this opportunity?

If you've been thinking about your next move, this could be a great opportunity to work within a site environment where you're connected to the studies, the people and the outcomes.

You'll have the chance to make a genuine contribution to early-phase clinical research while working alongside people who share your interest in delivering great trials.

And if you're currently working within a CRO and have been curious about moving to the site side, we'd love to hear from you too.

Interested?

You don't need to be actively looking to have a conversation.

If this sounds like something worth exploring, get in touch for a confidential chat.