Clinical Project Manager

About the Role

Accelagen is expanding their project management function, and currently looking for an experienced Clinical Project Manager in Australia

The Project Manager (PM) is the key client facing Accelagen representative. The PM is the primary contact for internal and external stakeholders relating to a clinical project.

The PM oversees specific project activities for the following team members Clinical Trial Lead, Senior Clinical Research Associates, Clinical Research Associates, Clinical Trial Assistant.

Key Responsibilities

• Project Management and Execution from project planning, initiation, recruitment, maintenance and close out
• Support Business Development activities by contributing to the development of budget proposals for prospective clients / projects
• Support with Business Development pre-award activities
• Set up and management of project timelines and key project deliverables.
• Facilitate a risk assessment for the project in conjunction with internal and external stakeholders.
• Identify and mitigate possible risk related events and routinely monitor study risk assessment and evaluation.
• Consult with and oversee progress of internal (cross-functional) stakeholders and activities within Accelagen scope from project start up, maintenance, close out to CSR delivery.

About You

You are an organised and detail-oriented professional who enjoys working in a collaborative environment and takes ownership of delivering high quality outcomes.

You will bring:

• Strong verbal and written communication skills.
• Excellent attention to detail and problem-solving abilities.
• A proactive, solutions-focused approach
• The ability to manage competing priorities and work independently.

Qualifications & Experience

• Life Sciences, Pharmacy, RN qualified or other technical qualification.
• PM: 3 years of Clinical Operations experience, demonstrating strong
• understanding of clinical trial management.
• Senior PM: Minimum 2 years of Project Management experience or a clear
• demonstration of the successful deliverable of projects which includes adherence to project timelines and successful maintenance of budget deliverables.
• Excellent knowledge of ICH-GCP and SAE and regulatory reporting
• Excellent communication skills
• Ability to work and display leadership within a project team

Why Join Accelagen?

At Accelagen, you'll be part of a collaborative and high-performing team supporting innovative clinical research across a diverse range of therapeutic areas. We offer opportunities for professional growth, flexible working arrangements, and the chance to make a meaningful impact on clinical trials that improve patient outcomes.

Ready to join us? Apply now and help shape the future of clinical research.