Scientific Director/Senior Medical Director, Medical Affairs - Eye Care
Company: AbbVie
Location: Irvine
Posted on: February 23, 2026
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Job Description:
Company Description 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 . Job Description Provides specialist medical and
scientific strategic and operational input into core medical
affairs activities such as: health-care professional and provider
interactions; generation of clinical and scientific data (enhancing
therapeutic benefit and value); educational initiatives (medical
education, scientific communications, and value proposition) and
safeguarding patient safety (risk minimization activities and
safety surveillance activities). Works closely with commercial
teams to provide strategic medical input into core brand (product)
strategies, and to support medical affairs, marketing activities
and market access. Drives MA input into and influences the
development of asset strategy. Provides specialist medical
insights, and executes on data generation, communication, and
expert engagement activities as deliverables to relevant ASTs for
both early and late stage development program including leading or
contributing to: comprehensive gap assessment, development of
Scientific Communication Platform, development of integrated
evidence plans to support launch readiness. Drives scientific
communication initiatives. Responsibilities: In collaboration with
Medical teams, Clinical Development, Commercial, Market Access,
HEOR and other functional areas, provides leadership, oversight,
and support for assigned indications/projects. Works closely with
Brand Teams and relevant cross-functional medical teams, to provide
strategic input into core asset strategy, and to drive medical
activities. Initiates medical affairs activities, generation and
dissemination of data supporting the overall scientific strategy.
Develops innovative research concepts for clinical data generation;
provides relevant scientific and technical training to internal
teams globally. Provides scientific and technical support for
assigned assets; delivers scientific presentations; develops and
maintains professional and credible relationships with key opinion
leaders; actively participates in relevant Asset, Development and
Pipeline Commercial cross-functional teams and drives the
development of medical affairs objectives aligned with strategy.
Provides scientific and technical input to inform the development
of the Asset Target Product Profiles (TPP). Provides input in
design and execution of Phase II-III trial programs including
target population and endpoint selection aligned with TPP. Works
cross functionally to lead the development of the asset Phase 3b/4
strategy. May assist in the development of scientifically accurate
marketing materials, medical education programs, advisories, and
symposia. Assists with the scientific review, development,
approval, execution, and communication of affiliate/area/global
medical affairs sponsored or supported clinical research
activities. May interact with and coordinate appropriate scientific
and medical activities with internal stakeholders (i.e.,
commercial, clinical operations, discovery, statistics, regulatory,
etc) as they relate to on-going medical affairs projects. Serves as
the scientific team interface for key regulatory discussions.
Provides scientific/medical education to investigators, clinical
monitors, and project team members related to therapeutic area or
disease specific information. Keeps abreast of professional
information and technology through conferences and/or medical
literature and acts as a therapeutic area resource. Lead functional
and cross functional teams responsible for discrete projects within
the specific therapeutic area (data analysis, expert engagement,
individual publications, study collaborations) Represents Medical
Affairs in due diligence activities for the acquisition of assets
aligned with the Disease Area Strategy. Ensures budgets, timelines,
compliance requirements are factored into programs' scientific
activities. Qualifications Scientific Director Qualifications:
Advanced Degree in sciences (PhD, PharmD, OD). Eye care experience
preferred. 7-10 years of experience in Medical Affairs with Global
Medical Affairs experience highly preferred. Typically, 10-15 years
of experience in the pharmaceutical industry or equivalent;
substantial understanding of relevant therapeutic area required.
Minimum of 4 years of clinical trials direct management experience
in the pharmaceutical industry or academia or equivalent. 4 years
of experience is preferred. Knowledge of clinical trial
methodology, data analysis and interpretation, regulatory
requirements governing clinical trials and experience in
development strategy and the design of protocols. Ability to run a
clinical study independently with little supervision. Proven
leadership skills in a cross-functional global team environment.
Must possess excellent oral and written English communication
skills. Senior Medical Director Qualifications: Medical Doctorate
(M.D.) degree or equivalent (D.O. or non-US equivalent of M.D).
Relevant therapeutic specialty in an academic or hospital
environment preferred. Completion of residency and/or fellowship is
preferred. Eye care experience preferred. Minimum of 2 years of
clinical trial or medical affairs experience in the pharmaceutical
industry or academia or equivalent. 5 years of experience is
preferred. Knowledge of clinical trial methodology, data analysis
and interpretation, regulatory requirements governing clinical
trials and experience in development strategy and the design of
protocols. Ability to run a clinical study independently with
little supervision. Proven leadership skills in a cross-functional
global team environment Ability to interact externally and
internally to support global business strategy. Must possess
excellent oral and written English communication skills. Additional
Information Applicable only to applicants applying to a position in
any location with pay disclosure requirements under state orlocal
law: The compensation range described below is the range of
possible base pay compensation that the Companybelieves ingood
faith it will pay for this role at the timeof this postingbased on
the job grade for this position.Individualcompensation paid within
this range will depend on many factors including geographic
location, andwemayultimatelypaymore orless than the posted range.
This range may bemodifiedin thefuture. We offer a comprehensive
package of benefits including paid time off (vacation, holidays,
sick),medical/dental/visioninsurance and 401(k) to
eligibleemployees. This job is eligible toparticipatein our
short-term incentiveprograms. Note: No amount of payis considered
to bewages or compensation until such amount is earned, vested,
anddeterminable.The amount and availability of any
bonus,commission, incentive, benefits, or any other form
ofcompensation and benefitsthat are allocable to a particular
employeeremainsin the Company's sole andabsolutediscretion unless
and until paidandmay bemodifiedat the Companys sole and absolute
discretion, consistent withapplicable 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
Keywords: AbbVie, Altadena , Scientific Director/Senior Medical Director, Medical Affairs - Eye Care, Healthcare , Irvine, California