23 ene
Parexel
Nuevo Casas Grandes
.Mexico, Remote**Job ID** R0000020546**Category** Clinical Trials**ABOUT THIS ROLE**:Parexel FSP is hiring multiple Site Care Partners to support the Mexico region-these are great opportunities for experienced CRAs seeking career advancement!
**Job Summary**The Site Care Partner is the main client 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 acts as a Subject Matter Expert aimed to optimize country and site selection activities by proactively collaborating with key stakeholders and providing local intelligence to country outreach surveys, investigator strategies and client pipeline opportunities.
The Site Care Partner is the "face of the client" and therefore accountable for ensuring that sites receive necessary support and engagement, issues are resolved, and the clientsreputation is upheld throughout study lifecycle.
Additionally, the Site Care Partner will coordinate with other roles and functions that will interface with study sites (eg.
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.
**Responsibilities**:- Accountable for site start-up and activation_- Deploy 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.- Supports the Feasibility Strategy and Analytics Lead to ensure that high quality feasibility results are delivered- Collaborate with key stakeholders providing country/regional level input to country outreach surveys including protocol feasibility, country SOC and medical practices (as applicable).- Provide country/regional level input to country strategy, feasibility, and protocol design in collaboration with relevant Medical Affairs colleagues,
and with input from external clinical experts as required.- 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
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