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Site Care Partner I

hace 2 meses

Alcobendas, Madrid, España Parexel A tiempo completo

**Job Summary**

The Site Care Partner I is a critical role at Parexel, responsible for ensuring the success of clinical trials at investigator sites. As the primary point of contact for sites, this individual will be accountable for building and maintaining strong relationships with investigators, resolving issues, and upholding the client's reputation.

**Key Responsibilities**

  • Provide input into site recommendations, leveraging intimate knowledge of country/region, sites, processes, and practices, as well as associated site performance metrics.
  • Support the Study Operations Manager/Global Study Manager in defining local requirements for the importation/exportation processes of investigational medical products and ancillary supplies.
  • Deploy Global Site and Study Operations (GSSO) site strategies by qualifying and activating assigned sites.
  • Collaborate with key stakeholders to provide country/regional level input to country outreach surveys, including protocol feasibility, country Standard of Care, and medical practices.
  • Maintain a thorough knowledge of assigned protocols and conduct study start-up activities at the site level, including PTA, site activation checklist items, ICD finalization, and Site Initiation Visit (SIV), as applicable.
  • Ensure all site initiation activities are completed, including training, documentation, and system requirements.
  • Support country-specific ICD review and deployment, as applicable.
  • Ensure follow-up activities are completed post-PTA and SIV to ensure site readiness for First Subject First Visit (FSFV).
  • Partner with site monitors to ensure site monitoring readiness in anticipation of FSFV.
  • Responsible for relationship building and operational oversight of the site, providing study support for escalated site issues related to study delivery.
  • Ensure the strategy/approach for Investigational Product (IP) and ancillary supplies for sites and country requirements throughout the lifecycle of the study.

**Requirements**

  • Strong understanding of clinical trials and site operations.
  • Excellent communication and relationship-building skills.
  • Ability to work independently and as part of a team.
  • Strong problem-solving and analytical skills.
  • Proficiency in Microsoft Office and other relevant software.

**Language**

English (en-US)