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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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cutting edge design and process development capabilities to accelerate and bring the best - in - class medicines to patients around the world. What You Will Achieve In your role, you will be at the center
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into actionable insights. PHYSICAL/MENTAL REQUIREMENTS Must be able to travel between Pfizer sites. NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS The position will requires approximately 20% travel
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