(Senior) Clinical Research Associate

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.

Qualifications:

• Educational Excellence:Bachelor’s degree in a scientific or healthcare discipline preferred.
• Experience Matters:At least 3 year of independent on-site monitoring experience.
• 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.