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About the Role:
- You will lead site activation activities to help clinical studies move forward efficiently and compliantly.
- You will be accountable for site activation strategy and execution from study start-up through completion.
What You'll Do:
- Oversee site activation deliverables and coordinate cross-functional teams to meet milestones.
- Manage the collection, tracking, and maintenance of essential study and site documentation.
- Communicate project status, risks, and updates to sponsors and study teams.
What You'll Bring:
- Bachelor's degree in a life science discipline and 4+ years in CRO or pharmaceutical industry.
- Strong understanding of ICH GCP, regulatory requirements, and clinical trial start-up processes.
- Excellent leadership, organizational, and stakeholder management skills.
Why Worldwide:
- Be part of a global team of clinicians, scientists, and researchers improving lives.
- Work remotely in Australia while collaborating with global teams across time zones.
Worldwide Clinical Trials
Worldwide Clinical Trials is a global contract research organization (CRO) dedicated to high-quality clinical research that brings life-changing therapies to patients. With more than 4,000 professionals worldwide, the company fosters a collaborative, inclusive culture where growth and innovation are encouraged.