Clinical Trial Coordinator

Job Title: Clinical Trial Coordinator

Location: Melbourne, Australia - onsite

Company Overview

We are partnering with one of Australia's leading Clinical Trial Networks, dedicated to conducting groundbreaking clinical trials that advance medical knowledge and patient care. With state-of-the-art facilities and a strong commitment to innovation, they offer leading project scopes across phases I-IV in diverse therapeutic areas.

You will be joining a growing site in Melbourne. This role would suit an experienced clinical trial coordinator looking to take on management responsibility.

Culture and Benefits

The company prioritises a people-centric culture, ensuring a collaborative and friendly approach to business.

They're a growing business and so offers a lot of progression opportunities for those joining.

Key Responsibilities:

• Plan and execute clinical trials, ensuring adherence to protocols, Good Clinical Practice (GCP), and regulatory requirements.
• Work closely with investigators, study teams, sponsors, and healthcare staff to ensure smooth trial operations.
• Prepare and submit applications to ethics committees and governance bodies, ensuring compliance with relevant standards.
• Manage recruitment, informed consent processes, scheduling, and monitoring of participants' progress.
• Maintain accurate trial records, prepare reports for stakeholders, and ensure documentation meets audit standards.
• Monitor timelines, budgets, milestones, and project deliverables effectively.
• Ensure all aspects of the trial meet high-quality standards, including data integrity and participant safety.
• Provide support and guidance to site staff on protocol delivery and trial procedures.

Qualifications & Experience:

• Nursing background OR Scientific Background
• Good Clinical Practice (GCP) certification is highly desirable to ensure compliance with ethical and regulatory standards.
• Experience coordinating clinical trials across various phases

Knowledge & Skills:

• Strong understanding of clinical research processes and regulatory requirements.
• Excellent organizational and communication skills.
• Ability to multitask, prioritize, and work well under pressure.
• Attention to detail and commitment to data integrity.
• Proficiency in electronic data capture systems and clinical trial management software.

Why Join?

This is a unique opportunity to contribute to innovative clinical trials in a supportive and forward-thinking environment. Our client offers a competitive salary, professional development opportunities, and the chance to work on cutting-edge research that has a real impact on patient outcomes.

How to Apply:

If you are an experienced clinical professional with a passion for clinical research and are ready to take on a challenging role in clinical trial coordination, we encourage you to apply.