Data Science Program Lead I
AbbVie · North Chicago, IL · 2 wk ago
Engineering$85k–$162k/yrFull-time
About the role
The Data Science Program Lead I is responsible for aligning Data Science and Statistical Sciences teams with program- and study-level strategies. They lead the DSS Study Team and represent DS as a member of the cross-functional study team. They act as a single point of contact and accountable operational lead for assigned studies, coordinating associated DSS study teams to meet operational objectives.
Responsibilities
- Aligns DSS study teams with program- and study-level strategies
- Leads the DSS Study Team and represents DS as a member of the cross-functional study team
- 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
- 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 âlessons learnedâ across functions
Requirements
- Bachelor's degree in business, management information systems, computer science, life sciences or equivalent. Master's preferred
- Must have at least 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
Qualifications
- None specified
Skills
- Strong understanding of clinical trial process and clinical technology
- Experience in managing a clinical trial from initiation through to completion
- Effective leadership skills
- Ability to influence others without direct authority
- Effective communication skills
- Effective analytical skills
Benefits
- Comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k)
- This job is eligible to participate in our short-term incentive programs
Pay
$84,500 - $162,000 USD
Schedule
Hybrid