Lead Clinical Study Coordinator / Site Manager

NES Fircroft; Melbourne; On-site; AUD 100,000 - 120,000; Full time

Job summary

A leading company is seeking an experienced Lead Clinical Study Coordinator/Site Manager to oversee clinical research operations in Melbourne. This role involves managing clinical site staff, ensuring compliance with regulations, and driving recruitment targets. Ideal candidates will have a nursing qualification, GCP training, and at least 5 years of experience in clinical trials. This position offers a platform to lead innovative research projects.

Qualifications

• Minimum 5 years’ experience in interventional clinical trials.
• GCP training and understanding of local regulatory requirements.

Responsibilities

• Lead and manage clinical site staff to ensure high-quality trial delivery.
• Collaborate with investigators and recruitment teams to achieve study goals.

Skills

Leadership

Team Management

Communication

Education

Nursing or health-related qualification

Certificate in Project Management

Tools

MS Office

Office 365

Job description

Lead Clinical Study Coordinator / Site Manager

Lead Clinical Study Coordinator / Site Manager

This range is provided by NES Fircroft. 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$120,000.00/yr

Direct message the job poster from NES Fircroft

NES Fircroft is seeking an experienced Lead Clinical Research Coordinator / Site Manager to lead clinical research operations at a dedicated clinical trials unit in Melbourne. This is an excellent opportunity to oversee the delivery of high-quality clinical trials while driving recruitment targets and optimising site performance.

Key Responsibilities

• Lead and manage clinical site staff to ensure high-quality trial delivery in compliance with GCP and regulatory standards
• Oversee site resources, recruitment targets, facilities, and equipment management
• Act as primary contact for sponsors and suppliers at site level
• Ensure staff training, performance management, and professional development
• Collaborate with investigators and recruitment teams to achieve study goals
• Drive operational efficiencies and continuous improvement in workflows
• Maintain strong relationships with service providers and healthcare facilities

Requirements

• Nursing or health-related qualification (diploma or bachelor’s degree)
• GCP training and understanding of local regulatory requirements
• Minimum 5 years’ experience in interventional clinical trials
• Solid understanding of the pharmaceutical and CRO industries
• Proven leadership and team management skills
• Competent with MS Office; experience with Office 365 is an advantage
• Certificate in Project Management

This role offers a fantastic platform to lead a dedicated clinical trials team and contribute to innovative research projects.

Apply now through NES Fircroft to explore this leadership opportunity in clinical research.

Seniority level

• Seniority level

  Mid-Senior level

Employment type

• Employment type

  Full-time

Job function

• Job function

  Research, Science, and Health Care Provider

• Industries

  Biotechnology Research, Medical Practices, and Research Services

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