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) 3+ years of management/supervisory experience Experience managing projects PHYSICAL/MENTAL REQUIREMENTS This position/role works in an office where physical requirements are consistent with typical
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May manage the study start up process in countries assigned (where SUPM not assigned) and/or oversee pCRO responsible for these activities as applicable Through the Site Care Partner/Country Trial
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, prioritize multiple demands, and effectively lead in a matrix organization. PHYSICAL/MENTAL REQUIREMENTS NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS Travel: approximately ~20% Attendance
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training slides and detailed information contained in the site Study Reference Manual. Provide support for queries and resolve issues from global study teams on the sample management process, including
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Sciences group by way of process improvement. Develop expertise navigating Pfizer compliance systems, registries (e.g. GDMS, pTMF, Clinical Trial Registries, etc.) and other study systems related
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compliance with good clinical practice (GCP), regulatory agencies, Institutional Review Boards (IRBs), and Pfizer processes. Apply knowledge gained within the Early Clinical Sciences group by way of process
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) 3+ years of management/supervisory experience Experience managing projects PHYSICAL/MENTAL REQUIREMENTS This position/role works in an office where physical requirements are consistent with typical
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set-up. Proactively coordinate with Clinical Scientists and Lead Clinician to assure understanding and agreement on deliverables throughout the process Provide input for the design of the Statistical
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process, strategic and tactical planning, and the foundational tools that support planning, communication, and continuous improvements in the area of operational delivery. JOB RESPONSIBILITIES Program
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submission execution, team effectiveness, resource management, risk management, and information and communication management. The GPM needs to have comprehensive understanding of the governance process