Associate Director of Statistical Programming

Main Location
New York City, NY, United States
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Bristol-Myers Squibb is a global Biopharma company committed to a single mission: to discover, develop, and deliver innovative medicines focused on helping millions of patients around the world in disease areas such as oncology, cardiovascular, immunoscience and fibrosis.

 

Join us and make a difference.  We hire the best people and provide them with a work environment that places a premium on diversity, integrity, collaboration and personal development. Through a culture of inclusion, we create a better, more productive work environment. We believe that the diverse experiences and perspectives of all our employees help to drive innovation and transformative business results.

Responsibilities

Project Responsibilities

  • Independently develops, troubleshoots,  and maintains complex programs and utilities in accordance with BDS’s software development lifecycle procedures
  • Provides comprehensive programming leadership and support to clinical development teams
  • Ensures quality of BDS deliverables by consistently applying analysis and reporting standards, and driving compliance with regulatory requirements, corporate and departmental SOPs and work practices
  • Drives the development and implementation of innovative strategies and technologies for clinical trial programming
  • Develops unambiguous and robust programming specifications for internal and external programming work
  • Provides technical guidance to statistical programmers and vendors around project conventions, standards, practices, and specifications to ensure integrated computing solutions
  • Reviews planning documents (e.g. statistical analysis plans, data presentation plans, data review plans) to ensure clarity, integrity and compliance with requirements and standards

Managerial Responsibilities

  • Effectively recruits, manages, develops, evaluates, rewards, motivates, and retains 3-5 direct reports, resulting in an increasing level of capabilities within BDS
  • Conducts objective setting, performance check-ins, and year-end discussions in compliance with BMS policies; aligns objectives, feedback and performance evaluation with the Director of Statistical Programming of ICF
  • Meets regularly with direct reports, focusing on project updates, development needs, issue resolution, and provides real-time coaching and feedback; holds staff accountable for quality and timeliness of programming activities; ensures staff is compliant with training requirements
  • Communicates with Director of Statistical Programming of ICF regarding promotions, performance concerns, and retention risks
  • Builds and maintains a network with stakeholders and peers to ensure cross-functional strategies and objectives intertwine and build upon each other to achieve results.
  • Models acceptable behaviors and communication with stakeholders to ensure effective partnerships
  • Serves as a point of escalation for technical, operational and staffing issues which are unable to be resolved at the team level
  • Enables a culture of inclusiveness, respect for diversity, compliance with processes; encourages the questioning and challenging of others in a respectful and constructive manner
  • Identifies, leads, and supports improvement initiatives within BDS and serves as a BDS representative on cross-functional initiatives

Qualifications

  • Graduate degree in statistics, biostatistics, mathematics, computer science or equivalent experience
  • Minimum of 10 years of clinical/statistical programming experience within pharmaceutical clinical development with experience that includes leading programming efforts to support regulatory filings (e.g. US, EU, Japan)
  • Minimum 5 years of experience in managing technical professionals in a regulated environment
  • Extensive knowledge of SAS software (i.e. Base, Stat, Graph components) and general computing techniques in addition to knowledge of R or other statistical software packages
  • Significant knowledge of the drug development process, clinical trial methodology, statistics and relevant regulatory requirements for drug approval
  • Demonstrated ability to operate and lead in a matrix organization, build successful working relationships and effective stakeholder management in an environment that requires diverse educational and functional expertise.
  • Able to adapt quickly to the changing needs of the organization
  • Able to organize multiple work assignments and establish priorities
  • Excellent verbal and written communications skills; able to communicate proactively and effectively

US military experience shall be considered towards industry and professional experience requirements.

Bristol-Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees the resources to pursue their goals, both at work and in their personal lives.

Mission
We're a community of women leveraging our connections into top companies to help underrepresented women get the roles they've always deserved. Simultaneously, we work to build truly inclusive hiring processes and environments where women can thrive and not just survive.
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Associate Director of Statistical Programming
Bristol Myers Squibb