Key Responsibilities

• Manage day-to-day administration and operations for ISRs and collaborative studies from concept approval to study closure:
  Partner with global, regional, and local Medical Affairs teams, Translational Medicine, Safety to review protocols and research plans
• To carry out budget analyses, regulatory submission support and contract negotiations
  Support clinical demand accuracy, clinical logistics preparation and Tech Ops readiness efforts by tracking institutional start up activities and ensuring timely progress
• Work with institutional contacts to reliably maintain study data in iEnvision platform to ensure single source of truth
• Proactively identify gaps in SOP and prepare updates to ERP playbook to address gaps or reflect process improvements and changes

Pay Range:$60 - $80

Preferred Qualifications

• Good understanding/experience in clinical and/or pre-clinical research, or experience in Clinical Research/Development, Medical Affairs
• PMP or equivalent project management qualification an advantage
  Affinity for a collaborative, team-oriented environment, and approach; ability to appropriately interact within Global Medical Affairs and across diverse departments, senior management, and external customers/vendors