Senior Clinical Research Associate I

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

📋 Description

• Conducts site qualification, initiation, interim monitoring, site management, and close-out visits (either onsite or remotely), ensuring adherence to regulatory standards, ICH-GCP, Good Pharmacoepidemiology Practices (GPP), and protocol compliance.

• Utilizes judgment and experience to assess the overall performance of the site and its staff, providing recommendations for site-specific actions; promptly communicates and escalates significant issues to the project team and formulates action plans.

• Maintains a thorough understanding of ICH/GCP Guidelines, relevant regulations, and company SOPs/processes.

⛳️ Requirements

• Bachelor's degree or equivalent qualifications in Life Sciences or a related field.

• A minimum of 4 years of independent clinical monitoring experience.

• Exceptional communication and interpersonal skills with both internal and external stakeholders.

• Strong time management abilities and the capacity for critical thinking.

• Full working rights in Australia or New Zealand (open to visa transfer sponsorship in Australia).

🏝️ Benefits

• Supportive and engaged line management.

• Training in technical and therapeutic areas.

• Peer recognition.

• Comprehensive total rewards program.