Manager, Global Scientific and Regulatory Documentation

Working with Bristol Myers Squibb, a pharmaceutical company, as a Manager, Global Scientific and Regulatory Documentation. The role involves leading document strategy and authoring regulatory documents in support of submissions and approvals in key markets and other geographies. The successful candidate will have a PhD/PharmD in a relevant scientific discipline or Master's/Bachelor's degree with 2-4 years of regulatory documentation experience.

Requirements

• PhD/PhD in a relevant scientific discipline or Master's/Bachelor's degree with approximately 2-4 years of regulatory documentation
• Strong writing skills in authoring and managing the production of IB, Safety Aggregate Report, Clinical Protocols, and/or CSR
• Ability to analyze and interpret complex data from a broad range of scientific disciplines
• Understanding of global pharmaceutical drug development
• Strong organizational, communication, facilitation, and interpersonal skills in a cross-functional team

Benefits

• Competitive benefits and services
• Additional incentive cash and stock opportunities
• Flexible work environment
• Opportunities for career growth and development