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New · posted Oct 31

AbbVie · Pharmaceuticals

Head of Asset in Respiratory, Immunology Clinical Development

  • North Chicago, IL
  • On-site
  • Full-time
  • VP & Executive
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EmploymentFull-time
DeadlineOpen until filled

The role

Manages other Medical and/or Scientific Directors and leads the direction, planning, execution, and interpretation of clinical trials or research activities of one or more clinical development programs. Participates in and may lead cross-functional teams to generate, deliver, and disseminate high-quality clinical data supporting overall product scientific and business strategy.

What you need

What you'll do

Personally or through a direct report, leads and demonstrates ownership of the design and implementation of multiple clinical development programs (or one large, complex program) in support of the overall product development plan, based on strong medical and scientific principles, knowledge of compliance and regulatory requirements, AbbVie’s customers, markets, business operations, and emerging issues. Oversees project-related education of investigators, study site personnel.

  • Has overall responsibility for leading and mentoring clinical study teams, monitoring overall study integrity, and review, interpretation, and communication of accumulating data pertaining to safety and efficacy of the molecule. Along with Clinical Operations, is responsible for ensuring agreed-upon study enrollment and overall timelines for key deliverables. Responsible for assessment and reporting of serious adverse events per corporate policy and regulations for those protocols assigned.
  • Has primary responsibility for and ownership of design, analysis, interpretation, and reporting of scientific content of protocols, Investigator Brochures, Clinical Study reports, regulatory submissions and responses, and other program documents.
  • Manages one level of Medical and Scientific Directors (typically 2 to 4) and/or Clinical Scientists. This responsibility involves direct oversight of clinical development activities and/or management of personnel who may be working on other projects. Responsible for hiring, onboarding, mentoring, training, and supporting career development of these individuals.
  • May chair Clinical Strategy Team(s), with responsibility for development of a rigorous, cross-functionally-aligned, vetted Clinical Development Plan with full consideration of contingencies and alternative approaches. In this capacity, responsibilities may include supervision of matrix team members and serving as the Clinical Research representative to lend clinical development and medical expertise to Asset Development Teams (ADTs) and ADT Leadership Boards (ALBs).
  • Serves as the in-house clinical expert for one or more molecules and diseases in the therapeutic area, coordinating and leading appropriate scientific activities with internal stakeholders as they relate to ongoing projects. May participate in or lead clinical development contributions to due diligence or other business development activity. As required by program needs, contributes in partnership with Discovery colleagues to design and implementation of translational strategies.
  • Acts as clinical lead and actively solicits opinion leader interactions related to the disease area(s); partners with Medical Affairs, Commercial and other functions in these activities as required, consistent with corporate policies, to ensure that broad cross-functional perspectives are incorporated into Clinical Development Plans and protocols as appropriate.
  • Stays abreast of professional information and technology through conferences, medical literature, and other available training, to augment expertise in the therapeutic area. May represent AbbVie at key external meetings.
  • Responsible for understanding the regulatory requirements related to the clinical studies and global drug development and accountable for complying with those requirements. Serves as a clinical representative for key regulatory discussions.
  • Ensures adherence to Good Clinical Practices, pharmacovigilance standards, standard operating procedures and to all other quality standards in conducting research.
  • Medical Doctor (M.D.), Doctor of Osteopathy (D.O.), or non-US equivalent of M.D. degree with relevant therapeutic specialty in an academic or hospital environment required. Completion of a residency program strongly preferred. Completion of a subspecialty fellowship is desirable.
  • At least 7 years (9+ years preferred) of clinical trial experience in the pharmaceutical industry, academia, or equivalent.
  • Respiratory experience strongly preferred.
  • Ability to run a complex clinical research program independently.
  • Proven leadership skills and ability to bring out the best in others on a cross-functional global team. Must be able to lead and manage through influence.
  • Demonstrated commitment to training and development of junior-level staff, using best judgment to assure that they work with an appropriate level of autonomy.
  • Ability to interact externally and internally to support a global scientific and business strategy.
  • Extensive knowledge of clinical trial methodology, regulatory and compliance requirements governing clinical trials, and experience in development of clinical strategy and the design of study protocols.
  • Must possess excellent oral and written English communication skills
  • Ability to exercise judgment and address complex problems and create solutions across multiple projects.

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 long-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.​

Pay and benefits

$248,000 – $472,000 a year

Employer provided
How this compares
  • Paid time off

  • Medical insurance

  • Dental insurance

  • Vision insurance

  • 401(k)

  • Long-term incentive programs

Where you'll work

North Chicago, ILOn-siteOpen in Maps (opens in a new tab)

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From the posting

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.

AbbVie company page · 109 open roles
Equal opportunity, accessibility and legal noticesAbbVie's statements, word for word

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 applicants seeking a reasonable accommodation, click here to learn more:

Job intelligence

The context around this role

Live data · October 31, 2026

Salary intelligence

How the pay compares

This role's midpoint is level with the US median for Clinical Development roles at this level.

This roleEmployer provided

$248,000 to $472,000 a year

VP & Executive roles in the US9 roles publishing pay

Middle half $340,000 to $400,000, median $360,000
Annual base pay
Annual base payLowMedianHigh
This role$248,000—$472,000
All US$340,000$360,000$400,000

This role: AbbVie's own published range. Comparisons: the base pay employers published on open Clinical Development roles at the same level on Regulatory Jobs, October 31, 2026. Nothing is estimated.

Career trajectory

Where this role sits in Clinical Development

The general path across 116 open Clinical Development roles on Regulatory Jobs, with the titles they carry most. Not AbbVie's own promotion track.

  1. Earlier

    Associate & Specialist

    Often: Summer Intern

  2. Earlier

    Senior & Principal

    Often: Clinical Scientist · Clinical Scientist/Sr. Clinical Scientist, Oncology

  3. Earlier

    Manager

    Often: Manager, Aesthetics Clinical Development · Senior Manager, Clinical Scientist

  4. One step back

    Director

    Often: Senior Director, Clinical Development · Executive Medical Director, Oncology Clinical Development

    $298K median96 open
  5. This role

    VP & Executive

    Often: Vice President, Clinical Development · Associate Vice President

    $360K median11 open

Skills DNA

What this role leans on

How many of the posting's 28 duty, requirement and summary lines touch each area. The posting's emphasis, not a proficiency score.

GMP and compliance: 4 linesLab testing and methods: 1 lineDocumentation and SOPs: 3 linesInvestigations and CAPA: 2 linesRegulatory submissions: 1 lineClinical trial conduct: 12 linesCollaboration and leadership: 11 linesGMPLab testingDocumentationInvestigationsSubmissionsClinical trialsTeamwork
  • Clinical trial conduct12
  • Collaboration and leadership11
  • GMP and compliance4
  • Documentation and SOPs3
  • Investigations and CAPA2
  • Lab testing and methods1
  • Regulatory submissions1

Regulatory intelligence

The rules behind this role

Frameworks and standards this posting's work falls under, matched from its own words, each linked to the official source.

Company hiring pulse

AbbVie on Regulatory Jobs

109
Open roles
61
Distinct roles
16
Locations

By discipline

  • Clinical60 55%
  • Quality25 23%
  • Regulatory24 22%

By level

  • Director56 51%
  • Manager24 22%
  • Senior & Principal13 12%
See all 109 AbbVie roles

More roles at AbbVie

All 109 AbbVie roles

Similar Clinical Development roles elsewhere

Head of Asset in Respiratory, Immunology Clinical Development at AbbVie

Open until filled. $248K–$472K a year, employer provided.

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