The Site Care Partner is the main point of contact for investigative sites throughout a study life cycle; accountable for site start-up activities through activation; accountable for building and retaining investigator site relationships and providing support from site recommendation through the lifecycle of studies; accountable for site-level recruitment and operational success, and accountable for safeguarding the quality and patient safety at the investigator site.  The Site Care Partner contributes to country and site selection activities by proactively collaborating with key stakeholders and providing local intelligence to country outreach surveys, investigator strategies and Pfizer pipeline opportunities under supervision.

The Site Care Partner is the “face of Pfizer” and therefore accountable for ensuring that sites receive necessary support and engagement, issues are resolved, and Pfizer’s reputation is upheld throughout study lifecycle.  Additionally, the Site Care Partner will coordinate with other roles and functions that will interface with study sites (e.g. Study Monitor, Investigator Contracts Lead, Site Activation Partner, Clinician, etc.) thereby, optimizing communications and enhancing overall visibility into and confidence of quality of site level activities.  The Site Care Partner is responsible for site oversight utilizing and interpreting data from analytic tools, in conjunction with country intelligence to proactively identify risks to quality and compliance and to develop and implement mitigation plans to address these risks.

What you will be doing:

• Accountable for site start-up and activationDeploy GSSO site strategies by qualifying and activating assigned sites
  Supports processes to optimize country & site selection activities including review and assessment of the draft potential site list & provide PTA output for site selection.
  Collaborate with key stakeholders providing country/regional level input to country outreach surveys including protocol feasibility, country SOC and medical practices (as applicable) under supervision.
  Maintain a thorough knowledge of assigned protocols
  Conduct study start up activities at the site level including but not limited to PTA, coordination of site activation checklist items, ICD finalization, SIV (as applicable), including management of issues that may compromise time to site activation.
  
• Accountable for study conduct and close-outAct as operational point of contact for all site-level questions, liaising with and escalating to appropriate teams to respond and resolve questions.
  Review Site Monitoring Reports
  Support the site with revision and submission of ICD documents (and amendments).
  Working with other roles, maintain system management (e.g., EDC , Shared Investigator Platform, Site Profile and other systems as applicable) at site level ensuring alignment across platforms.
  
• Responsible for proactively providing local intelligenceProvide input into site recommendations via intimate understanding of country/region, sites, processes and practices, and associated site performance metrics.
  Provide support to the Study Operations Manager/Global Study Manager to define local requirements for the importation/exportation processes of the investigational medical product and ancillary supplies.
  

Work Location Assignment: Remote - Field Based (U.K. only)