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Site Care Partner I
hace 2 meses
The Site Care Partner I is a key member of the Parexel team, responsible for ensuring the success of clinical trials at investigator sites. This role requires a strong understanding of site operations, regulatory requirements, and clinical trial management.
Key Responsibilities- Site Selection and Qualification: Provide input into site recommendations based on intimate knowledge of country/region, sites, processes, and practices, as well as associated site performance metrics.
- Site Activation and Start-Up: Deploy Global Site and Study Operations (GSSO) site strategies by qualifying and activating assigned sites, ensuring all necessary documentation and systems are in place.
- Site Monitoring and Oversight: Collaborate with site monitors to ensure site monitoring readiness and provide operational oversight of the site, ensuring effective site recruitment planning and delivery.
- Issue Resolution and Escalation: Provide study support for escalated site issues related to study delivery, coordinating communications and resolution efforts with vendors, sites, and other stakeholders.
- Regulatory Compliance and Quality Assurance: Ensure compliance with regulatory requirements and industry standards, maintaining a thorough knowledge of assigned protocols and ensuring the quality and patient safety at the investigator site.
To be successful in this role, you will need:
- Strong knowledge of clinical trial management, site operations, and regulatory requirements.
- Excellent communication and interpersonal skills, with the ability to build and maintain relationships with site staff, vendors, and other stakeholders.
- Ability to work independently and as part of a team, with a strong attention to detail and ability to prioritize tasks effectively.
- Strong analytical and problem-solving skills, with the ability to think critically and make sound judgments.
