Clinical Research Associate

4 weeks ago


Darwin, Northern Territory, Australia Pharmiweb Full time
Job Summary

As a Clinical Research Associate at Pharmiweb, you will be responsible for managing clinical trials within the Oncology department. Your primary focus will be on site activation, ensuring that all activities adhere to ICH-GCP guidelines and local regulatory standards. You will work closely with country operations teams to identify, select, and activate clinical trial sites. Your strong communication and influencing skills will enable you to effectively manage study sites both remotely and face-to-face.

Key Responsibilities

* Collaborate with country operations teams to identify and select clinical trial sites
* Perform Site Qualification Visits (SQVs) to assess site eligibility
* Build strong relationships with site personnel to facilitate a smooth onboarding process
* Ensure compliance with ICH-GCP guidelines, local regulatory standards, and internal SOPs
* Coordinate with country operations teams to collect essential documents for site activation
* Act as the main point of contact for sites, study teams, and external stakeholders

Requirements

* Bachelor's degree in Biological Sciences or equivalent
* Minimum 2-3 years' experience in monitoring pharmaceutical industry clinical trials
* Knowledge of several therapeutic areas, including Oncology
* Analytical/risk-based monitoring experience is an asset
* Strong communication and influencing skills
* Ability to operate and use various systems and databases

What We Offer

* Competitive salary range: $89,376.00 - $111,720.00 USD
* Annual leave entitlements
* Range of health insurance offerings
* Competitive retirement planning offerings
* Global Employee Assistance Programme
* Flexible country-specific optional benefits

About Us

At Pharmiweb, we value diversity, inclusion, and belonging. Our rich diversity makes us more innovative, enabling us to better serve our people, patients, customers, and communities. We're dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status.

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