Clinical Trial Coordinator

Job Title: Clinical Trial Coordinator - Senior or Team Lead

Location: Melbourne, Australia

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

• Good Clinical Practice (GCP) certification is highly desirable to ensure compliance with ethical and regulatory standards.

• Experience coordinating clinical trials across various phases (4 years)

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.

Be a part of pioneering research and contribute to the future of medicine.