Medical Director – Medical Affairs-Dermatology

Medical Director – Medical Affairs-Dermatology

Requirements

• Medical (MD / MBBS or equivalent)
• >7 years of medical affairs or clinical development experience
• Solid background and experience in drug development and life-cycle development of immunology related products
• Dermatology experience is required

Responsibilities

• Developing and leads all aspects of implementation of medical strategy and tactics, including scientific communications and publications, annual medical planning, field communications, and collaborations within the healthcare community
• Applying therapeutic/disease area expertise and business understanding to address current and future medical needs in clinical practice with medically appropriate use of investigational medicines
• Overseeing and provides hands on support in management, generation and dissemination of clinical and non-clinical data and results in high quality publications
• Acting as standing or ad-hoc member for various teams; provides scientific/medical perspectives to the global and US strategic and medical organizations
• Co-leads the formation, refinement and execution of a robust Phase 3b/4 plan
• Supporting the design, conduct, oversight, analysis and reporting of Medical Affairs clinical trials
• Ensuring timely submission and delivery of high-quality clinical trial documentation, implementation and execution
• Continuing to develop and cultivate long-term strategic partnerships with clinical experts, societies, collaborative groups, advocacy groups, and other external collaborators representing
• Prioritizing support of investigator-initiated studies and serves as a key member of internal Scientific Review Committees
• Ensuring accuracy of training material for scientific and product information
• Coordinating medical review and approval of promotional materials
• Ensuring goals and objectives are met and projects completed on time and within budget
• Is responsible for optimal medical affairs resource allocation across the spectrum of a product’s life cycle
• Oversees development and forecasting of project budgets across assets
• Champions high standards of compliance, ethics and patient safety, putting patients at the center of all actions
• Performs medical monitoring of post-registrational trials and is the signatory of documents related to interpretation of patient level data where necessary
• Interacts internally and externally with senior management and functional heads
• Represents Medical Affairs on the Strategic Product Team
• Works in a goal/objective oriented manner within formalized process to plan and implement annual goals in alignment with the corporate annual goals and core business strategy
• Potential to supervise Medical Directors and/or Associate Director

Preferred Qualifications

• Any alliance related setting experience is preferred
• Demonstrated experience leading technical and business discussions internally and externally and explain scientific/medical concepts to all levels
• Ability to cultivate and maintain relationships with leading medical/scientific experts in the relevant fields
• Ability to establish trust through the consistent demonstration of scientific expertise and follow-through on requests from key opinion leaders
• Strong leadership and management skills