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Site Relationship and Excellence Partner

Parexel International Corporation

Multiple Locations

******* REMOTE - US LOCATIONS - ALL US Locat*******The Site Relationship and Excellence Partner (SREP) is the main Client point of contact for investigative sites as well as accountable for safeguarding the quality and patient safety at the investigator siteThis role is responsible for site monitoring and oversight and building and retaining relationships from site activation through the lifecycle of studiesAs part of the oversight responsibilities, this role will utilize and interpret data from analytic tools, in conjunction with country and regional intelligence to proactively identify risks to quality and compliance and to develop and implement mitigation plans to address these risksThis role is also accountable for identifying Clinical Research Associate (CRA) performance issues and is responsible for ensuring appropriate corrective and preventative actions are put in placeThe SREP is the face of Client and therefore accountable for ensuring that sites receive necessary support and engagement, issues are resolved, and Client’s reputation is that of Partner of ChoiceThe SREP proactively collaborates and provides local intelligence to country outreach surveys, targeted sites strategies, study design, and Client pipeline opportunitiesThis role is accountable for study start up, activation, and execution to the plan for targeted sites. In addition to being the main point of contact, the lead will help coordinate with other roles and functions that will interface with target sites, thereby, simplifying site Client communications and enhancing overall visibility into and confidence of quality of site-level activitiesThe SREP should be capable of performing both the Site Excellence Partner and the Site Relationship Partner role as dictated by needAdditional Job DescriptionAdditional Job DescriptionThe Site Relationship and Excellence Partner (SREP) is the main Client point of contact for investigative sites as well as accountable for safeguarding the quality and patient safety at the investigator siteThis role is responsible for site monitoring and oversight and building and retaining relationships from site activation through the lifecycle of studiesAs part of the oversight responsibilities, this role will utilize and interpret data from analytic tools, in conjunction with country and regional intelligence to proactively identify risks to quality and compliance and to develop and implement mitigation plans to address these risksThis role is also accountable for identifying Clinical Research Associate (CRA) performance issues and is responsible for ensuring appropriate corrective and preventative actions are put in placeThe SREP is the face of Client and therefore accountable for ensuring that sites receive necessary support and engagement, issues are resolved, and Client’s reputation is that of Partner of ChoiceThe SREP proactively collaborates and provides local intelligence to country outreach surveys, targeted sites strategies, study design, and Client pipeline opportunitiesThis role is accountable for study start up, activation, and execution to the plan for targeted sites. In addition to being the main point of contact, the lead will help coordinate with other roles and functions that will interface with target sites, thereby, simplifying site Client communications and enhancing overall visibility into and confidence of quality of site-level activitiesThe SREP should be capable of performing both the Site Excellence Partner and the Site Relationship Partner role as dictated by need

Job Requirements:BS/BSc/MS/MSc or equivalent + 5 years of clinical research experience and/or quality management experienceSolid knowledge of clinical development processes with strong emphasis on monitoringDemonstrated ability to oversee a 3rd party and/or demonstrated ability in Quality Assurance (preferred)Site Management/Monitoring (CRA) experience (preferred)Ability to lead, troubleshoot and influence for deliveryDemonstrated knowledge of quality and regulatory requirements for applicable countriesDemonstrated experience in site activation

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Job posted: 2023-01-10

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