The Oncology Site Care Partner plays a vital role in establishing and maintaining productive relationships with investigative sites throughout the lifecycle of clinical studies. This position is essential for site start-up, activation, recruitment, and ensuring high-quality standards and patient safety. You'll leverage data analytics to identify and mitigate risks while collaborating with various teams to enhance site performance.

Key Responsibilities:
• Site Start-Up and Activation
• Implement client site strategies by selecting and activating assigned sites.
• Optimize site selection processes through thorough review and assessment of potential sites.
• Collaborate to deliver high-quality feasibility results.
• Provide input on country/regional outreach surveys regarding protocol feasibility and medical practices.
• Conduct study start-up tasks including qualifications, site activation checklists, and necessary documentation.
• Ensure site readiness for study initiation and monitor recruitment efforts.
• Build and maintain strong relationships with site organizations and strategic partners.
• Intelligence Gathering
• Provide insights into the site selection strategy based on understanding of local practices and site performance metrics.
• Support geographical expansion by exploring opportunities for collaboration.
• Assist in defining local requirements for the import/export of investigational products and materials.
• Study Conduct and Close-Out
• Review site reports and address related issues as necessary.
• Maintain ongoing assessments of site management to ensure compliance and efficiency.
• Educate investigator sites about upcoming client opportunities.
• Ensure effective communication and collaboration with Clinical Research Associates.
• Compliance with Standards
• Adhere to required training and maintain accurate administrative records.
• Stay updated on processes and regulatory requirements, including ICH-GCP guidelines.

Required Skills:
• Strong knowledge of Good Clinical Practice and regulatory requirements.
• Excellent communication and interpersonal skills.
• Proficiency with technology and adaptability to new systems.
• Ability to navigate and build cross-functional relationships effectively.

Experience and Education:
• Minimum of 5 years of site management experience, including as a Clinical Research Associate (CRA) in a clinical or pharmaceutical setting.
• Oncology experience is required, with demonstrated expertise in study start-up and close-out activities.
• Bachelor's degree or equivalent experience preferred; proficiency in local language and English is necessary.

Join us in making a significant impact in oncology clinical research! Apply today if you are driven to excel in a dynamic environment.