-
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
-
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
-
to inspection activities and regulatory agency questions. QUALIFICATIONS / SKILLS Education/Experience: Minimum 4+ years experience in regulated environment, or equivalent practical experience (pharmaceutical
-
, related to monitoring clinical trials, GCP, FDA, or country-specific regulatory environment Demonstrated success in prior scientific/technical/administrative roles Demonstrated experience in site activation
-
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
-
within the local clinical development environment with a goal to enhance Pfizer reputation in scientific leadership. Responsible for proactively providing local intelligence Provide country/regional level