Data Science Program Lead II/III

Summary

Join AbbVie's Data Science team, a best-in-class group responsible for generating business value from clinical trials data. This key role ensures successful delivery against program- and study-level accountabilities. You will align DSS study teams with program strategies, act as a single point of contact for assigned programs, and coordinate DSS study teams to meet objectives. Responsibilities include optimizing program execution, managing resources, tracking progress, and preparing reports. You will also ensure regulatory compliance and participate in inspections and audits, as well as coach and mentor team members. Leading innovation and process improvement initiatives is also a key part of this role.

Requirements

• Bachelor’s degree in business, management information systems, computer science, or life sciences
• 8+ years of pharma / clinical research / data management / health care experience or 10+ years of project management experience
• In-depth understanding of clinical trial processes and involved functional stakeholders, and clinical technology
• Management of a clinical trial from initiation through to completion in a lead role is required
• Demonstrated performance as a cross-functional leader
• Demonstrated ability to influence others without direct authority
• Demonstrated ability to successfully coach / mentor in a matrix environment
• Demonstrated effective communication skills
• Demonstrated effective analytical skills

Responsibilities

• Aligns DSS study teams with program- and study-level strategies. Supports governance of assigned programs and studies, both within and outside DSS. Assigned programs may include programs of any size or any complexity
• For assigned programs, acts as single point of contact and accountable operational lead from DSS. Coordinates associated DSS study teams to meet operational objectives. Engages and connects global functional and cross-functional teams at both the program and study levels Interacts with and influences all levels of management and cross-functional team members to achieve program objectives. Represents DS in cross-functional forums and, if assigned, leadership meetings
• Utilizes operational analytics and project management tools to optimize execution of programs and studies, to manage internal and external resources, to track study progress, and to prepare study status reports. Anticipates and identifies issues that could affect timelines of own, as well as studies managed by the team. Anticipates and identifies issues that could affect timelines or quality and develops options and solutions
• Ensure adherence to federal regulations and applicable local regulations, Good Clinical Practices (GCPs), ICH Guidelines, AbbVie Standard Operating Procedures (SOPs), and to functional quality standards. Stays abreast of new and/or evolving local regulations, guidelines and policies related to clinical development. Coordinates and participates as the DS study owner in regulatory inspections and internal quality audits
• Participates in oversight of vendors and provides feedback related to clinical trial operations, issues, and trends in performance
• Responsible for coaching and mentoring team members, as well as providing input into their development
• Leads DSS and cross-functional innovation and process improvement initiatives
• If assigned, responsible for identifying training needs and standardizing and facilitating training solutions for DS roles. Conducts “lessons learned” across functions
• May include direct and/or indirect supervision of staff, as well as contract resources

Preferred Qualifications

• Master’s degree
• PMP Certification or Lean Six Sigma Green Belt desired

Benefits

• Paid time off (vacation, holidays, sick)
• Medical/dental/vision insurance
• 401(k)
• Short-term incentive programs
• Long-term incentive programs