Responsible to ensure scientific pull through of key medical strategies into communications across multiple channels for Allergan Aesthetics Portfolio related to Body Contouring. Provides support for assigned products and is responsible for designing and implementing training content and programs, developing scientific resources for field medical and affiliates and leading strategic Medical projects while ensuring the highest level of clinical and business competency of the medical teams in support of organizational and franchise goals. Functions in a medical/scientific leadership role within assigned therapeutic area supporting on-market products, new indications/disease states, competitive intelligence and pipeline products. Maintains current therapeutic expertise necessary to serve as scientific, medical, and clinical expert to field medical teams/affiliates, TA teams, brand teams and R&D partners.
•Identifies Insight Trends: Address educational scientific gaps identified through the gathering of feedback from multiple field sources, compile and summarize to provide relevant insights. Communicate trends to the broader therapeutic team.
•Translates integrated brand plan into medical tactics and core communication topics: Responsible for designing a strategically aligned tactical plan, as appropriate for on market products, and pipeline products including new indications/disease states. Develops non-promotional field/affiliate resources and ensures communications are supported by medical communication standards, pharmacovigilance standards, SOP’s and all other quality and compliance standards in Medical Affairs.
•Provides input into externally facing materials for use : (i.e. Congress Booth, Ad Boards, Med Ed) with HCP or EE interactions (Payer, Patients, Prescribers, and Providers); educational initiatives (medical education, data, guidelines, and value proposition)
•Identifies, Designs and implements focused and impactful internal training programs: aiming to shape scientific understanding of etiology, mechanism of action, clinical trial data etc.
•Medical Material Review: Responsible for performing the accurate and detailed medical review of complex materials for assigned therapeutic area(s) within Medical Affairs. Provides timely and accurate reviews in accordance with established policies and practice standards, including regulatory guidelines to meet customer needs.
•Actively contributes to and drives medical and brand functional planning including: medical education, EE engagements; and provides strategic medical input into core brand/product strategies. Works with TA Lead to ensure external communication strategies and tactics align with both TA and Commercial Strategies.
•Scientific degree; advanced degree (e.g., MS, PhD, MD/DO, PharmD, NP, MSN) preferred.
•3-5 years of clinical, scientific/research, or industry related experience or equivalent required demonstrating strong leadership competencies and proven team-building skills with ability to lead in a global matrixed environment. Substantial understanding of relevant therapeutic area required.
•Knowledge of clinical trial design, results and methodology, regulatory and compliance requirements governing development of promotional and non-promotional materials is desirable.
•Ability to interact externally and internally to support global scientific and business strategy.
•Ability to independently evaluate risk and implement strategies that are compliant with applicable regulatory standards pertinent to the promotion of pharmaceutical products
•Demonstrated analytical, conceptual and administrative skills. Excellent communication skills (written and presentation).
•Flexibility and adaptability to organizational change and market demands. Ability to work in a fast-paced corporate environment. High sense of urgency and commitment to excellence in the successful achievement of objectives.
•Excellent planning and organizational skills. Ability to manage multiple priorities and ability to demonstrate good business judgment.
•Strong Project Management and Teamwork skills to address project risks and issues.
•Ability to influence without direct authority to effectively deliver cross-functional projects.
Significant Work Activities: N/A
Travel: Yes, 25 % of the Time
Job Type: Experienced