The Director provides strategic regulatory leadership for advertising, promotion, and scientific messaging to ensure compliance with FDA requirements across product lifecycles. They act as a key partner to cross-functional teams, leading the review of promotional materials and managing interactions with regulatory authorities.
The Senior Manager provides regulatory oversight for promotional materials, ensuring compliance with FDA regulations for direct-to-consumer and HCP communications. They act as a key partner in cross-functional review teams to manage product launches and lifecycle activities while identifying and mitigating regulatory risks.
The Area Sales Manager is responsible for leading, developing, and managing a high-performing sales team to achieve regional sales goals for the psychiatry portfolio. They will set strategic direction, provide individual coaching, and foster a collaborative team culture while managing market execution.
The Regional Business Director leads field-based sales teams to drive product sales and execute regional strategies within a defined geographical area. They are responsible for meeting financial goals, managing budgets, and developing talent through coaching and performance monitoring.
The Rare Epilepsy Market Lead is responsible for engaging with Centers of Excellence and HCPs to provide disease state education and promote specific epilepsy treatments. They will develop territory business plans, generate actionable market insights, and coordinate with cross-functional teams to improve patient outcomes.
Lead the strategic development and execution of scientific communication plans for Multiple System Atrophy to support launch readiness. Oversee publication planning, congress strategy, and the development of medical content while ensuring alignment across cross-functional teams.
Develop and implement US regulatory strategies to ensure the successful development and approval of drug and biological products. Act as the primary FDA contact and manage the preparation and submission of regulatory documentation throughout the product lifecycle.
