New · posted Oct 31
AbbVie · Pharmaceuticals
Manager, Aesthetics Clinical Development
- Irvine, CA
- On-site
- Full-time
- Manager
What you need
What you'll do
- Prepare scientific reports/presentations related to clinical trials using available software and templates and; review/contribute to clinical protocols, by utilizing expertise, to assist in interpretation of data.
- Coordinate advisory meeting agendas, activities and slide decks and consulting agreements
- Comply with procedures set forth in relevant IQS documents and Study protocols and other directives issued by the management regarding clinical studies.
- Lead the study development by applying most current electronic document conventions/processes most consistently/accurately to ensure scientific integrity of all processes.
- Responsible for receiving and completing tasks and assignments from function, Therapeutic Area MD or Scientific Staff within timeline with minimal supervision and; maximizing individual, function/therapeutic area and team productivity.
- Participate on teams for process improvement initiatives and review key decisions impacting project timelines with management.
- Apply experience to analyze clinical study data, including statistical data using available software to assist with ongoing blinded/un-blinded PK, safety and efficacy reviews and ensure the scientific integrity of all processes.
- Perform literature/competitive intelligence searches to recognize/resolve scientific and technical problems by applying the most current electronic document conventions and processes consistently and accurately.
- Provide/present key clinical study information to function/therapeutic area and management.
- May lead teams within therapeutic area and supervise exempt and/or non-exempt direct reports and mentor function/-therapeutic area personnel.
- Bachelors/Master’s degree, in Science related to Field with 11+ years’ experience in the pharmaceutical industry or Pharm-D/PhD with 1+years
- Ability to understand more complex clinical study principles
- Advanced understanding of appropriate technology necessary to analyze clinical study data, generate reports and create presentations, posters and manuscripts
- Experience in team, drug development, and scientific project leadership or related.
- Experience supporting clinical research, drug development and/or function/therapeutic area operations.
- Must have a proven record of successful projects.
- Experience in multi-faceted, broad-based multiple functions/therapeutic areas or clinical functions with in depth knowledge of clinical study issues.
- Ability to appropriately and effectively use resources to complete tasks and meet required timelines.
- Ability to produce work of the highest quality by paying attention to detail
- Must possess good oral and written communication skills
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.
US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html
Pay and benefits
$110,000 – $209,000 a year
Employer providedPaid time off
Medical insurance
Dental insurance
Vision insurance
401(k)
Long-term incentive programs
Where you'll work
Irvine, CAOn-siteOpen in Maps (opens in a new tab)
More jobs in Irvine, CA
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.
Purpose:
To build all necessary data/information needed in preparing internal documents/scientific reports
related to clinical trials and; to keep multiple reports moving forward simultaneously through multi-tasking.
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 · November 1, 2026
Salary intelligence
How the pay compares
This role's midpoint is 20% below the US median for Clinical Development roles at this level.
This roleEmployer provided
Manager roles in the US13 roles publishing pay
| Annual base pay | Low | Median | High |
|---|---|---|---|
| This role | $110,000 | — | $209,000 |
| All US (middle half) | $185,500 | $198,500 | $198,500 |
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, November 1, 2026. Nothing is estimated.
Career trajectory
Where this role sits in Clinical Development
The general path across 263 open Clinical Development roles on Regulatory Jobs, with the titles they carry most. Not AbbVie's own promotion track.
Skills DNA
What this role leans on
How many of the posting's 27 duty, requirement and summary lines touch each area. The posting's emphasis, not a proficiency score.
- Clinical trial conduct8
- Documentation and SOPs7
- Collaboration and leadership7
- Data and digital systems2
- Quality systems and risk1
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%
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Manager, Aesthetics Clinical Development at AbbVie
Open until filled. $110K–$209K a year, employer provided.