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to inspection activities and regulatory agency questions. QUALIFICATIONS / SKILLS Education/Experience: Minimum 4+ years experience in regulated environment, or equivalent practical experience (pharmaceutical
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and regulatory operations and environment in countries under responsibility English is required. Prior Experience Demonstrated clinical research experience and/or study management/startup project
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enhancement opportunities and quality improvements in the different R&D activity areas. Additional responsibilities include ongoing assessment and identification of external environment trends/best practices as
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as appropriate. PREFERRED QUALIFICATIONS Advanced degree (MS/MA) is preferred. Knowledge of data and/or document anonymization strongly preferred. NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT
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deadlines Creativity, resourcefulness, high energy and flexibility Excellent verbal and written communication skills. NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS Ability to travel 25
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in a collaborative environment with other units involved in clinical research. This position is being recruited in the following faculty titles, designation into the following title series will be
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and project/program issues and risks and drives resolution through a matrix environment, effectively documenting decisions/rationale. Partners with the Product Team Leader to prioritize asset level
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development plan. Facilitates the identification of operation and project/program issues and risks and drives resolution through a matrix environment, effectively documenting decisions/rationale. Partners with
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the ever-changing regulatory environment requires forward thinking and attention to detail. Your dedication and expertise will help expand and accelerate patient access to Pfizer medicines and vaccines
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respect for the environment and nature. Since its founding in 1868, Berkeley has fueled a perpetual renaissance, generating unparalleled intellectual, economic and social value in California