Site Care Partner I

hace 6 días

Alcobendas, Madrid, España Parexel A tiempo completo
Job Summary

Parexel is seeking a highly skilled Site Care Partner I to join our team. As the face of the client, this role is accountable for ensuring that sites receive necessary support and engagement, issues are resolved, and the client's reputation is upheld throughout the study lifecycle.

Key Responsibilities
  • Provides input into site recommendations via intimate understanding of country/region, sites, processes and practices, and associated site performance metrics.
  • Supports processes to optimize country & site selection activities including review and assessment of the draft potential site list & provide Pre-Trial Assessment (PTA) output for site selection.
  • Collaborates with key stakeholders providing country/regional level input to country outreach surveys including protocol feasibility, country Standard of Care and medical practices (as applicable) under supervision.
  • Maintains a thorough knowledge of assigned protocols and conducts study start-up activities at the site level including but not limited to PTA, coordination of site activation checklist items, Informed Consent Document (ICD) finalization, Site Initiation Visit (SIV), as applicable.
  • Ensures all the site initiation activity including training per site activation checklist, collect and complete necessary documentation/systems needed.
  • Supports country specific ICD review and deployment when applicable and ensures follow-up activities completed post PTA and SIV to ensure site readiness for First Subject First Visit (FSFV).
  • Partners with site monitor to ensure site monitoring readiness in anticipation of FSFV and responsible for relationship building and operational oversight of the site.
  • Provides study support for escalated site issues related to study delivery by coordinating communications and resolution efforts (e.g., vendor, site contracts and payment issues).
Requirements

The ideal candidate will have a strong understanding of clinical trial operations and site management, as well as excellent communication and interpersonal skills. They will be able to work effectively in a fast-paced environment and prioritize multiple tasks and deadlines.

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