The Associate Director, Real World Evidence Strategy is responsible for assessment of data needs/gaps, and identifying potential opportunities of using real world data to support all phases of drug development and commercial opportunities at Teva. Key activities include but are not limited to proactive identification and recommendation of new RWD sources and developing the road map for a state-of-the-art RWD ecosystem for Teva. In addition, the candidate will be responsible for developing and implementing RWE studies in collaboration with cross-functional team and identifying of opportunities for use with regulators, payers and for internal organizational insights, primarily relying on use of pharmacy, medical claims, digital, patient registries, and EHR data. The candidate will also be involved in the collaborative development, implementation and testing of ongoing analytical tool initiatives. The ideal candidate will bring strategic thinking expertise more so than the tactical execution of projects.
⦁ Assist in development of short, mid, long term road map for a state-of-the-art RWD ecosystem to maximize the use RWD/RWE across multiple stakeholders and across product life cycle.
⦁ Design an objective RWD assessment process that brings forward potential value and fit including recommendations on engagement: license, partner to build data products, projects only, or not engage
⦁ Develop and propose strategies to identify and employ innovative techniques to derive insights from structured and unstructured real-world databases.
⦁ Bring forward new data visualization ideas to convey insights effectively
⦁ Work collaboratively with RWD analytics function to independently lead Real world evidence and insights generation requests that are not assigned to HEOR and Epi leads (e.g., patient journey, generics/complex generics projects, commercial insights)
⦁ Keep abreast global trends and evolving regulatory, HTA, payer policy landscape with regard to acceptability and use of RWE for decision making
⦁ Interface with GHEOR and epi leads and other cross functional colleagues to plan work needed for optimal execution of team deliverables
⦁ Either alone or in partnership GHEOR lead and other scientists, develop/contribute to protocol /study report of real-world database studies
⦁ Help develop project plans, execute on deliverables within agreed upon timeframes, manage deadlines, communicate progress and make recommendations to address issues.
⦁ Effectively present results from rapid data queries/simple descriptive studies to collaborators
Candidate will be expected to work onsite in a hybrid environment three days a week at either the West Chester PA or Parsippany, NJ location.