Associate Director, Group Lead, Data Management Reporting and Analytics
Pfizer
Summary
You will bridge evidence-based medical decision support with colleagues and stakeholders to enhance health and treatment outcomes. Your work will be pivotal in ensuring that accurate, timely, and consistent data reaches clinical teams and other groups.
Job description
What You Will Achieve
- Set and manage objectives for high-complexity projects within the Global Business Unit Lead and allocate people, technology, and financial resources, including those outside direct authority
- Actively share knowledge across multiple functions and contribute to knowledge management processes
- Champion and develop resources for innovation, taking appropriate risks to implement new ideas
- Develop solutions for highly complex problems within the Global Business Unit
- Interpret the Division's strategy to establish and prioritize business goals
- Assess talent needs and identify potential talent within the organization
- Hold managers accountable for their management skills and the development of a diverse talent pipeline
- Lead teams to implement strategic directions and influence senior management decisions
- Partner with Global Business Unit leadership to achieve objectives and oversee operational activities to support the division's goals
Minimum Requirements
- BA/BS with at least 6 years of experience or MBA/MS with at least 5 years of experience or PhD/JD with at least 1 year of experience or MD/DVM with any years of experience
- Demonstrated relevant experience in pharmaceutical, biotech, Contract Research Organization (CRO), or Regulatory Agency
- Proven ability to manage complex projects and develop successful partnerships within and across functional areas
- Deep understanding of regulatory requirements and relevant data standards
- Strong communication, decision-making, influencing, negotiation, and project management skills
- Technical proficiency in using relational databases and data visualization tools
- Strong people management experience
Preferred Requirements
- Comprehensive knowledge and experience in CDISC (Clinical Data Interchange Standards Consortium)
- Experience with data management plans, including data preparation and validation activities
- Understanding of the drug development process and data operations required for the reporting of clinical trial data
- Ability to create data capture solutions that support the quality and timely delivery of data
- Ability to identify existing process and product improvements
- Experience using common AI tools, including generative technologies such as ChatGPT or Microsoft Copilot, to support problem solving and enhance productivity
- Demonstrated curiosity for exploring how these tools can improve outcomes and understanding of responsible AI practices, including risk management and ethical use
- Candidate demonstrates a breadth of diverse leadership experiences and capabilities including: the ability to influence and collaborate with peers, develop and coach others, oversee and guide the work of other colleagues to achieve meaningful outcomes and create business impact
Non-Standard Work Schedule, Travel or Environment Requirements
Ability to work during global hours to collaborate with colleagues in different time zones. Work Location Assignment: Hybrid
Requirements
- BA/BS with at least 6 years of experience or MBA/MS with at least 5 years of experience or PhD/JD with at least 1 year of experience or MD/DVM with any years of experience
- Demonstrated relevant experience in pharmaceutical, biotech, Contract Research Organization (CRO), or Regulatory Agency
- Proven ability to manage complex projects and develop successful partnerships within and across functional areas
- Deep understanding of regulatory requirements and relevant data standards
- Strong communication, decision-making, influencing, negotiation, and project management skills
- Technical proficiency in using relational databases and data visualization tools
- Strong people management experience
- Comprehensive knowledge and experience in CDISC (Clinical Data Interchange Standards Consortium)
- Experience with data management plans, including data preparation and validation activities
- Understanding of the drug development process and data operations required for the reporting of clinical trial data
- Ability to create data capture solutions that support the quality and timely delivery of data
- Ability to identify existing process and product improvements
- Experience using common AI tools, including generative technologies such as ChatGPT or Microsoft Copilot, to support problem solving and enhance productivity
- Demonstrated curiosity for exploring how these tools can improve outcomes and understanding of responsible AI practices, including risk management and ethical use
- Candidate demonstrates a breadth of diverse leadership experiences and capabilities including: the ability to influence and collaborate with peers, develop and coach others, oversee and guide the work of other colleagues to achieve meaningful outcomes and create business impact
Benefits
- 401(k) Matching
- Retirement Savings Contribution
- Paid Vacation
- Holiday & Personal Days
- Paid Caregiver/Parental Leave
- Medical Leave
- Medical, Dental & Vision
- Prescription Drug Coverage
- Long-Term Incentive Program
- Relocation Assistance
Company overview
Pfizer Inc. is an American multinational pharmaceutical and biotechnology corporation headquartered in New York City, founded in 1849 by German entrepreneurs Charles Pfizer and Charles F. Erhart. As one of the world's largest pharmaceutical companies, Pfizer develops and produces medications and vaccines across multiple therapeutic areas including immunology, oncology, cardiology, endocrinology, and neurology. The company is renowned for breakthrough drugs such as Lipitor, Viagra, and more recently, the Pfizer-BioNTech COVID-19 vaccine. With approximately 81,000 employees globally and operations in about 200 countries, Pfizer maintains 37 manufacturing sites worldwide. The company's current strategic focus includes oncology, rare diseases, and innovative vaccine development, while implementing significant cost-saving initiatives. Pfizer continues to advance its research pipeline with over 100 projects and maintains a strong commitment to scientific innovation and global healthcare access.