Thursday, 17th August 2023, Job by Parexel, GreenTodays :
Job Summary
- Published on: Thursday, 17th August 2023
- Designation: Site Care Partner (FSP)
- industry: Medical and Health
- Vacancy: 1
- Employment Status: Full-time
- Job Location: Aldershot
- Salary: 0
- Gender:
- Application Deadline: Thursday, 17th August 2023
Job Description
Job SummaryThe 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 clients reputation 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. Site Care Partner Level 2 may be expected to support Country Specific Activities that are required to assure end to end Clinical Trial Implementation (start up to close out).
Responsibilities + Skills
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.
Education
Bachelors degree or RN in a related field or equivalent combination of education, training and experience (estimate at least 7 years experience)
Experience