JOB SUMMARY
The 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 contributes to 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 under
supervision. 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 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 including

protocol feasibility, country SOC and medical practices (as applicable) under supervision.

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.

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 applicable.

Ensure follow up activities completion post PTA and SIV to ensure site readiness for FSFV

Partners with site monitor to ensure site monitoring readiness in anticipation of first subject first visit

Responsible for relationship building and operational oversight of the site

Provide 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 study.

Be 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

eg. recruitment, data entry timelines etc).

Partner with local RA/ CTRO / SAP to ensure timely completion on country / local registry when applicable.

Accountable for study conduct and close-out

Act 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 Reports.

Support 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 under DCSO/ Senior SCP supervision. In

addition, the SMO Assessment is reviewed and updated when major staffing, contracting, or other significant site

changes/issues occur to confirm that continuity and contingency plans are current.

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.

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 monitoring.

Drive monitoring efficiencies and best practices for study/region/program.

Support shaping 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 relationships.

Ensures clear and open communication with Study Operations Manager.

Support 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 intelligence.

Provide input into site recommendations via intimate understanding of country/region, sites, processes and

practices, and associated site performance metrics.

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 / SKILLS
Education
• Bachelor’s degree or RN in a related field or equivalent combination of education, training and experience (estimate
at least 5 years experience).

• Proficiency in local language preferred. English is required.
Experience
• Demonstrated experience in site management with prior experience as a 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.

Vaccines experience preferred.

Skills and Technical Competencies
• Knowledge of Good Clinical Practice/ICH Guidelines and other applicable regulatory requirements.
• Must demonstrate good computer skills and be able to embrace new technologies.
• Good communication, presentation, and interpersonal skills.
• Ability to manage required travel of up to 75% on a regular basis.
• 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.
Behavioral Competencies
• 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.

NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS

Travel position

Work Location Assignment: Remote

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The annual base salary for this position ranges from $93,500.00 to $155,900.00. In addition, this position is eligible for participation in Pfizer’s Global Performance Plan with a bonus target of 12.5% of the base salary and eligibility to participate in our share based long term incentive program. We offer comprehensive and generous benefits and programs to help our colleagues lead healthy lives and to support each of life’s moments. Benefits offered include a 401(k) plan with Pfizer Matching Contributions and an additional Pfizer Retirement Savings Contribution, paid vacation, holiday and personal days, paid caregiver/parental and medical leave, and health benefits to include medical, prescription drug, dental and vision coverage. Learn more at Pfizer Candidate Site – U.S. Benefits | (uscandidates.mypfizerbenefits.com). Pfizer compensation structures and benefit packages are aligned based on the location of hire. The United States salary range provided does not apply to Tampa, FL or any location outside of the United States.

Relocation assistance may be available based on business needs and/or eligibility.

Medical

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