Key Responsibilities
• Manage day-to-day administration and operations for ISRs and collaborative studies from concept approval to study closure:
• Plan the external project timeline and regularly monitor adherence, metrics, and progress throughout the study lifecycle
• Partner with global, regional, and local Medical Affairs teams, Translational Medicine, Safety to review protocols and research plans
• Work with partners to carry out budget analyses, regulatory submission support and contract negotiations
Basic Qualifications
Master’s and 4+ years of experience in the pharmaceutical industry/project management
OR
Bachelor’s with 6+ years of experience in the pharmaceutical industry/project management
OR
Associate and 8+ years of experience in the pharmaceutical industry/project management
OR
High School Diploma/GED and 10+ years of experience in the pharmaceutical industry/project management
