Global Site Activation Lead - Clinical Trials

Worldwide Clinical Trials; Australia; On-site; AUD 90,000 - 130,000; Full time

Job summary

Worldwide Clinical Trials in Australia seeks a Site Activation Lead to manage and deliver site activation across therapeutic areas. You will coordinate cross-functional teams, oversee site qualification, and ensure milestones are met within budget, aligning with GCP standards and SOPs.

The role requires at least four years in clinical research, strong leadership, and excellent communication. You will work with sponsors, sites, and internal stakeholders to drive successful study start-up while

Qualifications

• Minimum four-year college degree or equivalent education in life sciences or related field.
• Experience in clinical research (e.g., CRA, Reg Affairs) preferred.
• Proven ability to lead, plan, and deliver site activation activities with regulatory awareness.

Responsibilities

• Serve as primary point of communication for study start-up and maintenance activities.
• Oversee site activation activities to meet critical path milestones on time and within budget.
• Coordinate with functional groups involved in site activation and regulatory activities as applicable.
• Develop risk assessments and mitigation plans for site activation deliverables.
• Collaborate with sponsor, CPM, and project teams to report status and drive action.

Skills

Leadership

Organizational skills

Decision making

Interpersonal skills

Communication

MS Office

Cross-cultural comms

Education

Four-year college degree

Clinical research experience

Tools

MS Office

Digital systems aptitude

Job description

Worldwide Clinical Trials in Australia seeks a Site Activation Lead to manage and deliver site activation across therapeutic areas. You will coordinate cross-functional teams, oversee site qualification, and ensure milestones are met within budget, aligning with GCP standards and SOPs.

The role requires at least four years in clinical research, strong leadership, and excellent communication. You will work with sponsors, sites, and internal stakeholders to drive successful study start-up while