Global Site Activation Coordinator

Parexel; Australia; On-site; AUD 90,000 - 130,000; Full time

Job summary

Parexel in Australia is seeking a Site Activation Specialist to drive regulatory and site activation activities across clinical trials. You will coordinate documents, liaise with investigators, ethics committees, and client study teams to ensure timely initiation and ongoing trial support.

Key responsibilities include managing regulatory submissions, maintaining TMF, and supporting site audits. The role emphasizes collaboration, accuracy, and adherence to GCP and Parexel standards in a global

Qualifications

• Understanding of clinical research and GCP practices.
• Ability to manage regulatory submissions and approvals.
• Strong communication with study teams and sites.

Responsibilities

• Initiate and coordinate site activation activities.
• Prepare and submit regulatory documents within timelines.
• Coordinate with client and ethics committees for approvals.
• Maintain site documentation and TMF updates.
• Support site audits and inspections.
• Mentor new hires on processes and systems.

Skills

Clinical trial processes

Site activation

Regulatory documentation

Issue resolution

Cross-country coordination

Job description

Parexel in Australia is seeking a Site Activation Specialist to drive regulatory and site activation activities across clinical trials. You will coordinate documents, liaise with investigators, ethics committees, and client study teams to ensure timely initiation and ongoing trial support.

Key responsibilities include managing regulatory submissions, maintaining TMF, and supporting site audits. The role emphasizes collaboration, accuracy, and adherence to GCP and Parexel standards in a global