-
, and 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. What You
-
of assigned customers. Lead and/or manage a significant volume of projects developed in a field-based environment, while exhibiting the ability to prioritize, successfully implement, and demonstrate excellent
-
and regulatory operations and environment in countries under responsibility English is required. Prior Experience Demonstrated clinical research experience and/or study management/startup project
-
, and 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. What You
-
transparent environment that encourages strong partnerships and mutual trust between teams, sub-teams, and therapeutics areas. Accountable to multiple project/core study teams and clinical sub-teams and manages
-
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
-
understanding of medicine development to bear on all activities in partnership with cross-functional asset and medical partners. He/she is a part of a working environment where colleagues always understand and
-
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
-
environment, with ability to lead in parallel strategic and tactical tasks Strong analytical skills required to provide sound inputs into new partner product and financial evaluations Experience working with
-
analytical abilities and problem-solving skills. Ability to provide leadership, set priorities and be accountable to timeline . Training in a GCLP/GLP/GMP environment and other international regulatory