Lead Clinical Research Associate - Remote

Overview

The Lead Clinical Research Associate is responsible for managing and delivering full clinical site monitoring services for various projects, ensuring compliance with SOPs, study guidelines, and GCP best practices.

In Short

• Manage clinical site monitoring services for multiple projects.
• Design and oversee project monitoring services.
• Train and recruit site/patients.
• Manage site data and documentation.
• Monitor project site budgets and regulatory filings.
• Act as primary liaison between CRAs and project team.
• Participate in the development of project plans and protocols.
• Maintain collaborative relationships with stakeholders.
• Ensure compliance with GCP and SOPs.
• Work on multinational scale projects.

Requirements

• Experience in clinical site monitoring.
• Knowledge of GCP and regulatory requirements.
• Strong project management skills.
• Excellent communication and interpersonal skills.
• Ability to work independently and as part of a team.
• Experience in training and site recruitment.
• Proficiency in data management.
• Budget management experience.
• Ability to handle complex projects.
• Multinational project experience preferred.

Benefits

• Competitive salary.
• Opportunities for professional development.
• Collaborative work environment.
• Flexible working arrangements.
• Health and wellness programs.
• Supportive management.
• Access to industry conferences.
• Networking opportunities.
• Potential for career advancement.
• Comprehensive benefits package.