Clinical Research Associate

Description

• 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.

Qualifications

• Educational Excellence: Bachelor’s degree in a scientific or healthcare discipline preferred.
• Experience Matters: At least 4 years of on-site monitoring experience, with preference for oncology trials and haematology.
• Regulatory Savvy: Strong knowledge of GCP and ICH guidelines.
• Tech-Savvy: Proficiency in Microsoft Office and relevant technology.
• Communication Pro: Excellent written and verbal skills.
• Organized and Analytical: Strong organizational and problem-solving abilities.
• Time and Financial Management: Effective in managing time and finances.
• Team Player: Ability to build and maintain strong relationships with coworkers, managers, and clients.