Clinical Trial Project Manager

Company description:

Peter MacCallum Cancer Centre

Job description:

At Peter Mac we aim to continuously improve cancer care, research and education across all cancers and for all people affected by cancer: changing lives, breaking new ground. Everything we do is underpinned by our core values, Excellence, Compassion and Innovation. Welcoming people from a wide variety of different backgrounds and experiences is critical to fostering innovation, cultivating compassion, attracting and retaining top talent and providing the best possible cancer care for our patients.

YOUR ROLE IN OUR FUTURE

The Centre for Biostatistics and Clinical trials has been part of PMCC for 40 years and provides Investigator Initiated Trials with Statistical, Data Management and Project Management support to ensure quality trial delivery.

We are looking for a Clinical Trial Manager to join our growing team!

Key Benefits include:

• Competitive Salary

• 5 weeks annual leave

• Accrued Days off

• Generous Salary Sacrifice

In your role as a Clinical Trial Project Manager you will work as part of a dynamic cross functional team and support investigator lead Clinical Trials to support delivery of alternative treatment options and better the lives of those impacted with cancer.

You will be responsible for driving the cross functional team to both meet timelines as well as quality deliverables.

If you are a CRA looking to step into a Project Management Role or a Project Manager looking for a local position, with the ability to interact directly with Investigators and make a real difference, this role is for you!

Your core responsibilities will be:

• Develop project plan, metrics and timelines for new projects in collaboration with C/PI, biostatistics and data management.

• Coordinate and assist in the development, review and amendment of study protocols, manuals, PICFs

• Collaborate with internal and external stakeholders and lead the study team to ensure study milestones are met

• Ensure delivery of the study is as per protocol, study plans, ICH GCP guidelines, SOPs

• Contribute to process improvements across the department

• Oversight and management of Clinical Trial safety reporting requirements as per protocol, relevant regulations and guidelines

• HREC and governance submission preparation, review and management

• Coordination and project management of Clinical Trial operational, logistics and service provider requirements as required e.g. laboratory, pharmacy, CROs

Key Selection Criteria:

• Degree in Health, Life Science, Science, or related field

• Previously experience in CRO, Pharmaceutical, Biotech company, academic Clinical Trial organisation or equivalent

• Experience in at least one of the following:

• Clinical protocol and CRF development

• Clinical trial set-up, coordination, and project management

• Clinical trial data management and reporting

• Demonstrated understanding of Good Clinical Practice, regulatory, ethical, privacy and other relevant guidelines.

• Project management skills including the ability to work with minimal supervision across multiple projects and tight timelines.

• Excellent written and oral communication skills.

• Ability to working as an effective member of a multi-disciplinary team.

• Ability to create cooperation and support from collaborators from diverse backgrounds and experiences.

• Understanding of medical terminology.

• Sound computer skills.

Applicants to this role should provide a covering letter outlining relative key skills and experience to assist us with our assessment.

Hiring Manager: Jacqui Cumming
Contact Number: 03 8559 7***
Email: **************@petermac.org

Applications Close: 11:59 pm 17th April 2024