# Site Care Partner **Company**: Pfizer **Work arrangement**: remote **Experience**: senior **Job type**: full-time **Salary**: $116,000.00 to $193,400.00 **Category**: Healthcare **Industry**: Healthcare **Apply**: https://pfizer.wd1.myworkdayjobs.com/en-US/PfizerCareers/job/United-States---New-York---New-York-City/Site-Care-Partner-II_4966262?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply **Canonical**: https://yubhub.co/jobs/job_f426cec6-95e ## Description The Site Care Partner is a key Pfizer point of contact for investigative sites throughout a study life cycle. 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 - Collaborate with key stakeholders providing country/regional level input to country outreach surveys - Provide country/regional level input to country strategy, feasibility and protocol design - Maintain a knowledge of assigned protocols - Conduct study start up activities at the site level including PTA, coordination of site activation checklist items, ICD finalization, SIV - Ensure all the site initiation activity including training per site activation checklist, collect and / complete necessary documentation/ systems needed for site activation - Support country specific ICD review and deployment when applicable - Ensure follow up activities’completion post PTA and SIV to ensure site readiness for FSFV - Responsible for relationship building and operational quality of the site - Provide study support on escalated site issues related to study delivery - Ensure the strategy/approach for IP and ancillary supplies for sites and country requirement throughout the lifecycle of the study - Be accountable for effective site recruitment planning and delivery - Partner with local RA/ CTRO / SAP to ensure timely completion on country / local registry when applicable - Responsible for establishing and maintaining relationships with Site Organizations and Strategic Partners Accountable for study conduct and close-out: - Review Site Reports and related issues - During the conduct of the study, the Site Management Organization Assessment is reviewed with the site - Inform and educate investigator sites of Pfizer pipeline opportunities - Support development and delivery including issue resolution of decentralized capabilities at investigator sites - Demonstrate leadership within the local clinical development environment - 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 - Ensures clear and open communication with Study Operations Manager - Support the CRA/site monitor to develop positive Investigator relationships Responsible for proactively providing local intelligence: - Provide input into country strategy/planning and site recommendations - Provide input to cluster level intelligence for site strategy and support implementation of cluster-level strategy - Provide 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: - Bachelor’s degree or RN in a related field or equivalent combination of education, training and experience: least 7 years’ experience - Ability to manage required travel - Proficiency in local language preferred, English is required - Demonstrated experience in site management with prior experience as a CRA/ Site monitor - Demonstrated experience in start-up activities through to site activation - Demonstrated experience in conduct and close out activities - Demonstrated knowledge of quality and regulatory requirements in applicable countries - Knowledge of Good Clinical Practice/ICH Guidelines and other applicable regulatory requirements - Excellent communication, presentation and interpersonal skills - Demonstrated networking and relationship building skills - Demonstrated ability to manage cross functional relationships - Ability to communicate effectively and appropriately with internal & external stakeholders - Ability to adapt to changing technologies and processes - Knowledge of country requirements for GCP that may be different to those of Pfizer Procedures - Effectively overcoming barriers encountered during the implementation of new processes and systems - Identifies and builds effective relationships with investigator site staff and other stakeholders - Effective verbal and written communication skills in relating to colleagues and associates both inside and outside of the organization - Effective in managing cross functional relationships ## Skills ### Required - Good Clinical Practice - ICH Guidelines - regulatory requirements - site management - relationship building - communication skills ### Nice to have - Oncology therapeutic area - local language proficiency --- Source: [Apply at pfizer.wd1.myworkdayjobs.com](https://pfizer.wd1.myworkdayjobs.com/en-US/PfizerCareers/job/United-States---New-York---New-York-City/Site-Care-Partner-II_4966262?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply)