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 study guidelines and 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 SOPs and GCP best practices.
• Work in an in-house based position.

Requirements

• Experience in clinical site monitoring.
• Knowledge of GCP and SOPs.
• Strong project management skills.
• Excellent communication skills.
• Ability to manage budgets and regulatory filings.
• Experience in training and recruitment.
• Ability to work collaboratively with stakeholders.
• Detail-oriented with strong organizational skills.
• Ability to work on multinational projects.
• Proficient in data management.

Benefits

• Competitive salary.
• Health and wellness benefits.
• Opportunities for professional development.
• Collaborative work environment.
• Flexible working hours.
• Supportive team culture.
• Access to the latest tools and technologies.
• Potential for career advancement.
• Work-life balance initiatives.
• Employee recognition programs.