TheAssociate Director, Biostatistics will serve as educator/advisor to the GlobalMedical community on the strengths/opportunities and limitations of trialdesigns, statistical methods, data collection approaches and the formulation ofkey scientific messages from clinical information.
Participate in the review and approval of Investigator Sponsored trials and BMS sponsored Phase IV trials (including post marketing commitments).
Enable and contribute to effective presentations to be made to Health Care Providers , including key investigators, payers and at scientific conferences/congresses.
Collaborate with regional Health Economics and Market Access Teams on identifying analysis methods and interpretation of observation data and other real world type data (such as Patient Registries and Claims Data Bases).
Effectively communicates the Global Biometric Sciences (GBS) Mission and Vision in a fashion that generates pride, excitement and commitment within GBS and the GMT.
Invests in developing knowledge outside of traditional statistical expertise in the clinical, regulatory and commercial environments.
Together with the GBS Planning and Execution Lead, identifies project resource needs, and, in coordination with the development team, aligns team's approved objectives and timelines with the GBS project level book of work and the allocation of external vendor resources to ensure effective delivery.
Effectively communicates with internal scientific governance bodies (e.
CSC), clinical and commercial partners, external opinion leaders and manages relationships and interactions with development alliance partners.
Builds the external reputation of BMS R&D via external interactions (academic relationships, conference presentations, governmental research organization reviewer, etc).
Contributes to GBS strategic initiatives through participation on initiative teams and/or contributing in feedback sessions.
Qualifications Significant academic training in statistics, biostatistics or arelated quantitative field.
PhD degree in statistics or biostatistics orMaster's degree with relevant experience preferred.
7 - 9 years of experience in planning and managing statisticalaspects of clinical research and reporting of clinical trials.
Experience withobservational data preferred.
Statistical expertise, medical/clinical trials knowledge, andproject management skills.
Excellent verbal and written communications skills.
Strong interpersonal skills evidenced in interactions withindividuals at all levels of the organization, and demonstrated ability todevelop relationships within the organization and leverage the formal andinformal organizational structure to assist in goal achievement, including theresolution of conflicts or their appropriate escalation.
Bristol-Myers Squibb is an equal opportunity employer - M/F/Vet/DisabilityRequisition ID - 1501123

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