AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok.

• Aligns DSS study teams with program- and study-level strategies.
• For assigned studies, leads the DSS Study Team and represents DS as a member of the cross-functional study team
• For assigned studies, 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 Interacts with and influences cross-functional team members to achieve program and study objectives
• 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 or quality and develops options and solutions
• Ensures 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
• Participates in oversight of vendors and provides feedback related to study operations, issues, and trends in performance Responsible for coaching and mentoring Data Science Associates. 
• May include indirect supervision of work for contract resources Participates in DSS and cross-functional innovation and process improvement initiatives Contributes to study execution “lessons learned” across functions

• Bachelor’s degree in business, management information systems, computer science, life sciences or equivalent. Master’s preferred.
• PMP Certification or Lean Six Sigma Green Belt desired Must have at 3+ years of pharma / clinical research / data management / health care experience or 5+ years of project management experience (and / or applicable work experience) Strong understanding of clinical trial process and clinical technology.
• Experience in managing a clinical trial from initiation through to completion is preferred Demonstrated effective leadership skills。
• Demonstrated ability to influence others without direct authority Demonstrated effective communication skills.
• Demonstrated effective analytical skills

AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community.  Equal Opportunity Employer/Veterans/Disabled. 

US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html

US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:

https://www.abbvie.com/join-us/reasonable-accommodations.html