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Senior Clinical Research Professional

7 days ago

Melbourne, Victoria, Australia IQVIA Argentina Full time
Job Description

We are currently seeking a highly skilled and experienced Clinical Research Associate (CRA) to join our sponsor-dedicated team.

This dynamic role offers the opportunity to drive innovation and excellence in clinical research, ensuring that study sites not only meet but exceed regulatory compliance standards.

As a key member of our team, you will be responsible for site visits, recruitment strategies, training, and documentation management. Your expertise will contribute to the success of our studies, making a tangible impact on project outcomes.

Key Responsibilities:
  • Engage in Site Visits: From selection to close-out, your visits will be pivotal in ensuring the success of our studies.
  • Recruitment Strategies: Develop and implement innovative plans to recruit study subjects, making a tangible impact on project outcomes.
  • Empower Sites with Knowledge: Provide essential training and maintain robust communication channels to keep sites aligned and motivated.
  • Champion Quality and Integrity: Evaluate and enhance site practices, ensuring adherence to protocols and regulations.
  • Drive Study Progress: Monitor every aspect of the study, from regulatory submissions to data query resolutions, ensuring seamless execution.
  • Master Documentation: Keep meticulous records and ensure all site documents are perfectly maintained.

You must have a minimum of 4 years Independent on-site monitoring experience to be considered for this role.