This is a fully remote position, open to applicants in Australia.

📋 Description

• Oversee clinical trial locations to guarantee compliance with study protocols, regulatory mandates, and Good Clinical Practice (GCP) benchmarks.

• Perform site visits to evaluate site performance, address challenges, and offer assistance for effective trial implementation.

• Collaborate with interdisciplinary teams to ensure prompt and precise data gathering and reporting.

• Deliver training and support to site personnel and fellow Clinical Research Associates (CRAs).

• Establish and nurture strong relationships with site staff and stakeholders to ensure seamless trial operations.

• Partner with a leading biopharmaceutical company across a diverse range of medicines and vaccines.

⛳️ Requirements

• Advanced degree in a pertinent field such as life sciences, nursing, or medicine.

• Significant experience as a Clinical Research Associate in Australia, with a deep understanding of clinical trial workflows and regulatory standards.

• Demonstrated capability to manage multiple sites and projects concurrently, showcasing strong organizational and problem-solving abilities.

• Proficiency in monitoring practices, data integrity, and site management, along with expertise in relevant clinical trial software and tools.

• Exceptional communication, interpersonal, and stakeholder management skills, with the capacity to influence and promote compliance in a complex setting.

• Willingness to travel at least 60% of the time (both internationally and domestically - by air and road).

• Valid driver's license.

• Legal authorization to work in Australia.