Clinical Research Associate

Please note as part of the assessment you will be asked to complete a short video screening interview.

Essential Functions:

• 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.
• Collaborate and Innovate: Work closely with a passionate team to support project execution and drive success.
• Manage Finances with Precision: Oversee site financials and ensure timely invoice retrieval.

What You Bring

• A degree in life sciences or healthcare (or equivalent experience).
• 18 months minimum on-site Independant monitoring experience to be considered, ideally oncology or Heamatolgy
• Deep knowledge of GCP, ICH, and clinical trial operations.
• Tech-savvy with Microsoft Office and mobile tools (iPhone/iPad).
• A proactive mindset, strong communication skills, and a passion for excellence.

Why Join Us?

• Work on diverse, global studies across multiple therapeutic areas.
• Be part of a supportive, innovative team that values your growth.
• Enjoy flexible work arrangements, travel opportunities, and career develop