AbbVie Posted August 20, 2026

Clinical Data Strategy and Operations Program Lead I - Immunology- HYBRID

Irvine, CA Full-time
Clinical Development Immunology

AbbVie is the source of truth for this posting and owns the application process. We surface normalized context and market comparison you won't find on the original listing.

About this opportunity

Company Description

About AbbVie

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 including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at  www.abbvie.com . Follow @abbvie on  LinkedIn,   Facebook ,  Instagram ,  X  and  YouTube.

Job Description

AbbVie Data Science is the best-in-class team within its cross-industry peer group and is responsible for bringing people, process, and technology together to generate business value from clinical trials data. Our operational model is exemplified through execution and innovation. This role is key to ensuring successful delivery against the program- and study-level accountabilities assigned to Clinical Data Strategy and Operations (CDSO).

Responsibilities

Aligns CDSO study teams with program- and study-level strategies. For assigned studies, leads the CDSO 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 CDSO. Coordinates associated CDSO 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 CDSO and cross-functional innovation and process improvement initiatives.

Contributes to study execution “lessons learned” across functions.

Qualifications

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

Additional Information

​Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law: ​

The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future. ​

We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.​

This job is eligible to participate in our short-term incentive programs. ​

Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of  any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and may be modified at the Company’s sole and absolute discretion, consistent with applicable law.

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

Job details

Seniority
Not listed
Function
Clinical Development
Therapeutic area
Immunology
Location
Irvine, CA
Employment type
Full-time

How this role compares

Computed from every other active Clinical Development role in our database, not just this employer's listings.

We currently track 964 comparable Clinical Development roles across 91 biopharma companies.

964Comparable roles tracked
897Currently active
91Companies hiring similar roles
39Countries represented

Salary context

346 of 964 peers report a salary range (USD, annualized)

Peers share this role's job function. This posting doesn't list a seniority level, so peers aren't narrowed by seniority either -- the range below may span more levels than usual.

This roleSubject $75,000/yr – $142,500/yr
Lowest disclosed · Patient Safety Epidemiology Associate Director · Vertex Pharmaceuticals Inc (US) $0/hr – $0/hr (≈ $0–$0/yr)
Peer group range $0 – $458,800 (median $222,900)

Where these roles are based

Top locations among the 964 comparable roles

United States495
India143
United Kingdom57
China38
Poland35
Japan23

+ 33 more countries

Seniority mix

769 of 964 peers have a known seniority level

Manager204
Director181
Senior114
Associate Director102
Associate58
Executive/VP40
Senior Director38
Principal29
Intern/Fellow/Postdoc3

Therapeutic area mix

203 of 964 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Oncology92
Immunology38
Neuroscience26
Cardiovascular / CVRM15
Respiratory12
Ophthalmology8
Dermatology & Aesthetics5
Vaccines & Infectious Disease3
Rare Disease3
Gastroenterology1

Similar opportunities

The closest matches from our peer group, ranked by how similar they are, not how well you'd qualify for them -- treat this as market context, not a guaranteed shortlist; a weak match is labeled as one below.

80%similar
Lilly Indianapolis, Indiana, United States of America
Same function Same therapeutic area Same country
80%similar
AbbVie North Chicago, IL Director
Same function Same therapeutic area Same country
80%similar
AbbVie North Chicago, IL Executive/VP
Same function Same therapeutic area Same country
80%similar
AbbVie Director
Same function Same therapeutic area Same country

Open in 2 locations

North Chicago, United StatesWaltham, United States
80%similar
AbbVie Director
Same function Same therapeutic area Same country

Open in 2 locations

Waltham, United StatesSouth San Francisco, United States
80%similar
E.R. Squibb & Sons,L.L.C. Princeton, United States Director
Same function Same therapeutic area Same country

Notify me about similar jobs

Get an email when we spot other openings like this one – same job function, comparable seniority, roles you'd actually want to see.

How we calculate "similar"

No black box, no LLM guesswork: a deterministic score built from four normalized attributes. Here's this role's own peer group at different match levels, so you can see the mechanism, not just the result.

Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.

80%
Clinical Research Lead - Immunology, Investigator Engagement (CA-West Coast Region)
Lilly · Indianapolis, Indiana, United States of America · Seniority not listed
Function Therapeutic area Seniority Country
80%
Medical Director, Immunology Clinical Development
AbbVie · North Chicago, IL · Director
Function Therapeutic area Seniority Country
80%
Director, Clinical Pharmacology (Immunology)
AbbVie · Waltham, MA · Director
Function Therapeutic area Seniority Country
80%
Clinical Research Director - Immunology and Inflammation
Sanofi US Services Inc. · Cambridge, United States · Director
Function Therapeutic area Seniority Country
Unmatched or unknown dimensions score exactly the same: 0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.