Description:
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.