Sr. Information Manager - Modeling & Simulation ( Sr. Manager )

This position sits within the Clinical Trial Solutions (CTS)- Information Management organization.  This role will support the Center of Excellence (CoE) and their partners including Clinical Pharmacology, Statistics, and our Clinical Programming teams.  The individual in this position will be responsible for partnering with the above lines to define and deliver a common clinical sciences platform in support of Pfizer's model informed drug development (MIDD). ROLE RESPONSIBILITIES Support or serve as business lead on the implementation and management of systems and support processes and its partners using industry standard methodologies. Serve as an subject matter expert to support the functional business lines Serve on cross-functional broad and strategic initiatives and solutions that can be applied to enhance existing solutions or to the introduction of new systems or processes. Consult across CTS and its partners on all aspects of information use, including retrieval, analysis, integration, organization and management. Draw on broad knowledge of existing solutions and interrelationships to provide ad-hoc consulting on CTS and enterprise-wide projects as required. Support information management solutions novel to the pharmaceutical industry which may include solutions in support of modeling and simulation, real world evidence, statistical analysis. QUALIFICATIONS Education:  Bachelor or Master (preferred) Degree in Statistics, Data Sciences, Biological Sciences, Computer Sciences, or related field. Prior Experience: 8-12years experience in a related field. Experience with modeling and simulation techniques and tools for integrating data, knowledge, and mechanisms to aid in arriving at rational decisions regarding drug use and development.  Experience with Nonmem a plus. Excellent understanding of machine learning techniques and algorithms. Experience with common data science toolkits, such as SAS, R, and Python,  Hands on experience in at least one of these is highly desirable. Experience in use, leading business facing implementations and/or support of technologies used in Clinical Pharmacology, Statistics and Clinical Programming. Knowledge/understanding of technologies to support clinical trials, familiarity with software development lifecycle; understanding of the state-of the-art technologies to evaluate and leverage them into improved business processes for worldwide deployment and adoption. Technical Competencies: Demonstrated ability to work on multiple projects. Demonstrated knowledge of clinical development process including in depth knowledge and understanding of the principles of GCP. Demonstrated project management skills as well as effective verbal and written communication skills in relating to colleagues and associates both inside and outside the organization. Proven ability to define clear, streamlined processes for technologies supporting clinical trials. Understand customers and stakeholders and adapt messages appropriately. Ability to make complex decisions that require choosing between multiple options. Ability to work in ambiguous situations within the team to identify and resolve complex problems. Ability to organize tasks, time and priorities of self and others; ability to multi-task. 4721433
Salary Range: NA
Minimum Qualification
8 - 10 years

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