Sr. Clinical Research Associate - Remote

Overview

This position involves managing and delivering full clinical site monitoring services for various projects, ensuring compliance with guidelines and best practices.

In Short

• Manage clinical site monitoring services for multiple projects.
• Design and oversee project monitoring services.
• Responsible for site/patient recruitment and data management.
• 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.
• Ensure compliance with SOPs and GCP best practices.
• Maintain collaborative relationships with stakeholders.
• In-house based position.
• May involve complex and multinational projects.

Requirements

• Experience in clinical site monitoring.
• Knowledge of GCP and regulatory requirements.
• Strong project management skills.
• Ability to manage budgets and regulatory filings.
• Excellent communication and interpersonal skills.
• Experience in training and oversight of CRAs.
• Ability to work collaboratively with stakeholders.
• Detail-oriented with strong organizational skills.
• Ability to handle complex projects.
• Experience in multinational project management is a plus.

Benefits

• Opportunity to work on complex projects.
• Collaborative work environment.
• Professional development opportunities.
• Competitive salary and benefits.
• In-house training and support.