Clinical Project Manager

Accelagen Pty Ltd; Sydney; On-site; AUD 140,000 - 180,000; Full time

Job summary

Accelagen Pty Ltd is expanding its clinical project management function in Sydney. The Clinical Project Manager will be the primary Accelagen contact for internal and external stakeholders, overseeing activities from startup to CSR delivery across the trial team.

You will coordinate timelines, budgets and risk assessments, while supporting business development efforts and maintaining high-quality project outcomes in collaboration with a dedicated team across Clinical Trial Lead, SCRAs and CRAs.

Qualifications

• PM/Clinical Operations experience with strong trial knowledge.
• ICH-GCP and SAE regulatory reporting knowledge.
• Leadership within a cross-functional project team.
• Experience delivering projects on time and within budget.

Responsibilities

• Lead project planning, initiation, recruitment, maintenance and close out.
• Set up and manage project timelines and deliverables.
• Support business development activities and budget proposals.
• Coordinate with internal and external stakeholders across Accelagen.
• Identify and mitigate project risks and monitor risk assessments.

Skills

Communication

Attention to detail

Problem-solving

Prioritization

Education

Life Sciences/Pharmacy/RN or equivalent

Job description

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
• 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.