Clinical Project Manager

Our client, a boutique Australian Clinical Trial Site, is looking for an experienced CPM to join the team, where you will manage a variety of complex trials.

Enjoy the benefits of working in a close-knit team, where your contributions are valued, and you have full autonomy over your projects. They are a genuine employee-centric business, dedicated to progressive working solutions to ensure employees feel valued and supportive. We have placed many people into the team over the years and have had continuously positive feedback.

With flexible remote working arrangements, you can achieve a healthy work-life balance without the demands of US or EU hours - while still gaining the experience managing full end-to-end of projects in a smaller business environment.

They have some ambitious growth plans coming into 2024/2025 and so you will be apart of a successful expanding business, this presents many opportunities to grow within the team and offer faster progression pathways.

Key Responsibilities:

• Lead the planning, execution, and oversight of complex oncology clinical trials, ensuring adherence to time-lines, budget, and quality standards.
• Serve as the primary point of contact for clients, investigators, and vendors, fostering strong relationships and effective communication throughout the project lifecycle.
• Develop and implement strategic plans and innovative approaches to optimise study performance and address challenges in oncology research.
• Collaborate with cross-functional teams to identify and mitigate risks, proactively resolve issues, and ensure successful project outcomes.
• Provide leadership and guidance to project team members, promoting a culture of excellence, collaboration, and continuous improvement.
• Actively participate in business development activities, including proposal development and client presentations, to support the growth of the oncology portfolio.

Qualifications:

• Bachelor's degree in life sciences or related field; advanced degree preferred.
• Minimum of 3 years of experience in clinical project management within a CRO or clinical site setting.
• Proven track record of successfully managing complex clinical trials from start-up to close-out, including experience with study start-up activities, site management, and data management.
• Excellent communication, leadership, and interpersonal skills, with the ability to effectively collaborate with internal and external stakeholders.

Why Join:

• Opportunity to work in a small business environment with a genuine interest in implementing new strategies and change management processes.
• Close-knit culture that values collaboration, innovation, and professional development.
• Flexible remote working arrangements, allowing for a healthy work-life balance.
• Chance to work on complex oncology studies and make a meaningful impact in the field of oncology research.
• Competitive compensation package including salary, bonus, and benefits.

Title: Clinical Project Manager

Location: Melbourne, on-site/hybrid

Salary: $125,000 - $155,000 plus superannuation (dependent on experience)

To apply, please submit your resume directly or contact Keeley Munday for more information at kmunday@i-pharmconsulting.com

Please note: Due to high level of applicants, only those successful will be contacted.