[U390] - Site Care Partner Senior Manager

Detalles del empleo
Tipo de empleo: Jornada completa
Ubicación: Madrid, Madrid provincia
Descripción completa del empleoThe Site Care Partner is the main Pfizer 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 Pfizer pipeline opportunities. 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 (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.
JOB RESPONSIBILITIESAccountable for site start-up and activationDeploy GSSO site strategies by qualifying and activating assigned sitesSupports 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 deliveredCollaborate 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 protocolsConduct 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.Ensure all the site initiation activity including training per site activation checklist, collect and / complete necessary documentation/ systems needed for site activation (e.g. PSR, SART, ESRA, SAC, FU Letter, Planisware, ISF/eISF etc.)Support country specific ICD review and deployment when applicableEnsure follow up activities completion post PTA and SIV to ensure site readiness for FSFVPartners with site monitor to ensure site monitoring readiness in anticipation of first subject first visitResponsible for relationship building and operational oversight of the siteProvide study support on escalated site issues related to study delivery by coordinating communications and resolution efforts (e.g., vendor, site contracts and payment issues etc.)Ensure the strategy/approach for IP and ancillary supplies for sites and country requirement throughout the lifecycle of the studyBe accountable for effective site recruitment planning and delivery, consistent with global and/or country plan and local targets: Responsible for enrollment support and ensure progress by responding to recruitment issues from investigators.Maintain regular communications with investigator sites to gather status updates and drive delivery to study goals (e.g. recruitment, data entry timelines etc).Partner with local RA/ CTRO / SAP to ensure timely completion on country / local registry when applicableAccountable 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 ReportsSupport 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.During the conduct of the study, the Site Management Organization Assessment is reviewed with the site, when applicable, on an annual basis following site initiation and updated as needed.Review and manage site practices that differ from Pfizer practices and liaise with study management and Business Process Owners as needed.Maintain regular communications with investigator sites to gather status updates, informal and formal performance metrics, and study-level feedback.Inform and educate investigator sites of Pfizer pipeline opportunities that may be a good fit.Oversight and management of site deliverables to study targets, i.e. data cuts/sweeps, interim analyses, database locks, helping to oversee data is up to date and any other site-facing deliverables, i.e. investigator signatures.Follow the study oversight plan and proactively put in place mitigations for known/anticipated risks.Support development and delivery including issue resolution of decentralized capabilities at investigator sites e.g. home health, ePRO, DTP etc.Assure quality and consistency in the delivery of monitoringDrive monitoring efficiencies and best practices for study/region/programDemonstrate leadership within the local clinical development environment with a goal to enhance Pfizer reputation in scientific leadership.May act as a Subject Matter Expert on Pfizer systems and processes.Actively pursue possible efficiencies and develop best practices in the delivery of activities for site performance throughout the life cycle to increase investigator/site satisfaction and strengthen site relationshipsEnsures clear and open communication with Study Operations ManagerSupport the site monitor to develop positive Investigator relationships throughout the life of the study and escalate any training or compliance concerns with Country Trials Manager and Study Management.Responsible for proactively providing local intelligenceProvide input into country strategy/planning and site recommendations via intimate understanding of country/region, sites, processes and practices, and associated site performance metrics.Provide input to cluster level intelligence for site strategy and support implementation of cluster-level strategy in collaboration with the Study Operations Manager/Global Study ManagerProvide regional exploration/territory development growing adjacent opportunities where possible.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.QUALIFICATIONS / SKILLSEducation:
Bachelor's degree or RN in a related field or equivalent combination of education, training and experience (estimate at least 7 years experience)Proficiency in local language preferred. English is requiredExperience:
Demonstrated experience in site management with prior experience as a site monitorDemonstrated experience in start up activities through to site activationDemonstrated experience in conduct and close out activitiesDemonstrated knowledge of quality and regulatory requirements in applicable countriesSkills and Technical Competencies:
Knowledge of Good Clinical Practice/ICH Guidelines and other applicable regulatory requirementsMust demonstrate good computer skills and be able to embrace new technologiesExcellent communication, presentation and interpersonal skillsAbility to manage required travel of up to 75% on a regular basisDemonstrated networking and relationship building skillsDemonstrated ability to manage cross functional relationshipsAbility to communicate effectively and appropriately with internal & external stakeholdersAbility to adapt to changing technologies and processesKnowledge of country requirements for GCP that may be different to those of Pfizer ProceduresBehavioral Competencies:
Effectively overcoming barriers encountered during the implementation of new processes and systemsIdentifies and builds effective relationships with investigator site staff and other stakeholdersEffective verbal and written communication skills in relating to colleagues and associates both inside and outside of the organizationORGANIZATIONAL RELATIONSHIPSDirect Report to DCSO (or Site Care Partner/FSP Line Manager)
Indirect relationships with:
Global Study Manager/Study Operations ManagerStart Up PMSAP-CTACTROPurposeBreakthroughs that change patients' lives... At Pfizer we are a patient centric company, guided by our four values: courage, joy, equity and excellence. Our breakthrough culture lends itself to our dedication to transforming millions of lives.
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Disability InclusionOur mission is unleashing the power of all our people and we are proud to be a disability inclusive employer, ensuring equal employment opportunities for all candidates. We encourage you to put your best self forward with the knowledge and trust that we will make any reasonable adjustments to support your application and future career. Your journey with Pfizer starts here!
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