This range is provided by i-Pharm Consulting.
Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.
Base pay range A$100,000.00/yr - A$115,000.00/yr
Principal Consultant at i-Pharm Consulting | Recruiting Clinical Operations, Clinical Project Management and Biometrics Professionals across Australia Job Title : Team Lead Clinical Trial Coordinator
Location : Sydney, 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.
Culture and Benefits
The company prioritises a people-centric culture, ensuring a collaborative and friendly approach to business.
Team members often enjoy lunches together and benefit from a range of incentives.
Key Responsibilities :
Lead the planning and execution of 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 National Health and Medical Research Council (NHMRC) standards.
Oversee recruitment, informed consent processes, scheduling, and monitoring of participants' progress.
Maintain accurate trial records, prepare reports for stakeholders, and ensure documentation meets audit standards.
Manage timelines, budgets, milestones, and project deliverables effectively.
Ensure that all aspects of the trial meet high-quality standards, including data integrity and participant safety.
Provide guidance and training to site staff on protocol delivery and trial procedures.
Knowledge & Skills :
A bachelor's degree in a relevant field such as Nursing, Medical Science, Life Sciences, Public Health, or Clinical Research is typically required.
Good Clinical Practice (GCP) certification is highly desirable to ensure compliance with ethical and regulatory standards.
At least 5 years of experience coordinating or managing clinical trials across various phases (I-IV), with a proven track record in leadership roles.
Why Join?
This is a unique opportunity to lead 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 leadership role, we encourage you to apply.
Feel free to reach out to Keeley Munday at .
Be a part of pioneering research and contribute to the future of medicine!
Seniority level Mid-Senior level
Employment type Full-time
Job function Management, Research, and Other
Industries Pharmaceutical Manufacturing, Biotechnology Research, and Research Services
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