Site Care Partner (Lead Clinical Research Associate) - Oncology - Remote

Overview

The Site Care Partner I (SCP I) is responsible for ensuring that clinical trial sites receive necessary support and engagement, resolving issues, and maintaining the client's reputation throughout the study lifecycle.

In Short

• Act as the main client point of contact for investigative sites.
• Oversee site start-up activities through to activation.
• Build and retain investigator site relationships.
• Ensure quality and patient safety at investigator sites.
• Support site recruitment and operational success.
• Collaborate with key stakeholders for site selection.
• Conduct study start-up activities including site initiation visits.
• Manage communications and resolve escalated site issues.
• Review site monitoring reports and ensure compliance.
• Coordinate with various roles to enhance site-level activities.

Requirements

• 5+ years of experience as a site monitor, specifically in Oncology.
• Proven experience in start-up activities through to site activation.
• Knowledge of quality and regulatory requirements.
• Strong computer skills and adaptability to new technologies.
• Effective communication skills with internal and external stakeholders.
• Networking and relationship-building skills.
• Ability to manage cross-functional relationships.
• Willingness to travel up to 75% regularly.
• Bachelor's Degree or Registered Nurse.
• Demonstrated ability to overcome barriers in process implementation.

Benefits

• Opportunity to contribute to improving global health.
• Work within a supportive and empathetic team environment.
• Access to comprehensive drug development capabilities.
• Work with a globally recognized CRO.
• Engagement in diverse clinical development solutions.