Jobs / United States / Abbvie INC
Manager, Clinical Outcome Assessment Digital Implementation Team Navigator
Abbvie INC · 🇺🇸 North Chicago, IL, US
Sponsorship verdict
Sponsorship possible
One solid signal, not two — worth applying, and worth asking about sponsorship early.
- Employer is on a government sponsor recordThe US Department of Labor certified 177 H-1B/E-3 labor condition applications for this employer between Oct 2025 and Jun 2026 (latest Jun 2026) — the step every H-1B hire needs first. USCIS also records 94 H-1B approvals in FY2023. Source: LCA disclosure data (US Department of Labor (OFLC)).
- The posting doesn’t mention sponsorshipSilence isn’t a refusal — ask the recruiter before investing much time.
- No salary bar for this routeH-1B has no fixed salary bar: the employer must pay at least the prevailing wage for the role and area. Cap-subject employers enter a lottery weighted by wage level. Source: https://www.federalregister.gov/documents/2025/12/29/2025-23853/weighted-selection-process-for-registrants-and-petitioners-seeking-to-file-cap-subject-h-1b, rules effective 2026-02-27.
- What Abbvie INC paid sponsored hires in similar roles2 certified filings for “Manager, Business and Digital Analytics” (Data Scientists) in IL: $149k–$169k, median $159k. Most were filed at wage level III (50%) — 3 lottery entries, ≈46% projected selection odds for cap-subject employers. Source: US Department of Labor LCA disclosure data (Oct 2025 – Jun 2026).
- Confirmed live todayWhen a source last listed this job as open.
US H-1B: cap-subject employers enter a lottery weighted by wage level — Level I gets 1 entry, Level IV gets 4 (DHS projected selection odds ≈15% at Level I to ≈61% at Level IV). Universities and non-profit research employers are cap-exempt. The $100,000 fee for new petitions from abroad is currently blocked by a court order (appeal pending).
A verdict summarises public evidence; it is not legal advice and never a guarantee — the employer and the immigration authority decide. Sign in to factor in where you can already work.
Or apply yourself on the official page →
Sponsor Radar — Abbvie INC
The US Department of Labor certified 177 H-1B/E-3 labor condition applications for this employer between Oct 2025 and Jun 2026 (latest Jun 2026) — the step every H-1B hire needs first. USCIS also records 94 H-1B approvals in FY2023. Source: LCA disclosure data (US Department of Labor (OFLC)).
Past sponsorship or register membership never guarantees sponsorship for this vacancy or for you. Full Sponsor Radar for Abbvie INC →
About the role
The Clinical Outcome Assessment Digital Implementation Team (CDIT) Navigator serves as the strategic lead for Clinical Outcome Assessment (COA) licensing, translation, and implementation activities across assigned therapeutic areas, driving early stakeholder alignment, proactive study planning, risk mitigation, and successful end-to-end delivery. Responsibilities • Provides strategic expertise to the organization in support of program level COA licensing and translation implementation. • Directs enterprise strategic delivery of COA activities to support therapeutic area study teams: o Serves as a key business partner for the asset team leader in developing core strategies and meeting program goals; o Serves as a resource to study teams in the early stage development of COA strategies by providing strategic expertise and oversight for COA licensing, translations, and intelligence; o Develops and maintains CDIT TA strategic account plan in support of TA goals; • o Partners with HEOR and CSL to proactively identify COA needs and requirements for upcoming clinical programs and trials; o Participates with cross-functional teams to liaison with oversight committees, such as IEST, as needed; o Forecasts needs for COAs at program level by partnering with TA program team leaders and asset team leaders; and o Operates with a strategic, cross-functional mindset regarding COA licensing and translation implementation. • Responsible for partnering with CDIT Team PM and study teams: o Coordinates CDIT TA program management team deliverables utilizing scoping meetings to set direction for study teams; o Supports the CDIT program manager in driving cross-functional alignment within study team; o Mentors CDIT TA program manager to develop key messages and navigate good decision-making processes to effectively manage study team meetings; o Ensures appropriate incorporation of intelligence from strategic account plan • o Ensures high performance of CDIT TA program management team by defining KPIs for key COA activities and continuous monitoring and assessment of teams’ performance and providing feedback to ensure KPIs are met; and o Ensures appropriate CDIT document management practices are followed and repository of key program information is maintained. • Proactively identifies challenges or potential issues for execution within program COA strategies and COA study team plans, serving as key point in escalation of issues, as needed. • Actively champions and seeks opportunities to improve effectiveness the COA end-to-end development process: o Proactively seeks learnings from other teams and shares best practices; o Partners with cross-functional colleagues and study teams to seek process improvement opportunities; o Participates as needed in developing and implementing change; and • o Responsible for building and maintaining relationships with external stakeholders to enable effective implementation of the end-to-end process, such as translation vendors and external copyright holders. • Responsible for hiring, coaching, managing, training, onboarding, growth, and development of their direct reports. • Bachelor's Degree in a scientific field or equivalent; or equivalent with relevant experience is acceptable. • (Preferred) At least 6 years (and/or applicable work experience) in clinical research, demonstrating a high level of core, technical, and leadership competencies, through setting and driving strategy and leading cross-functional collaborations. • Experience effectively working in a matrixed organization. • Experience in both global and regional teams in the pharmaceutical industry. • Strong program management skills and knowledge of program management practices in the pharmaceutical industry and common tools utiliz