| Company Name: |
AbbVie |
| Location: |
North Chicago, IL |
| Position Type: |
Full Time |
| Post Date: |
03/06/2026 |
| Expire Date: |
04/05/2026 |
| Job Categories: |
Advertising/Marketing/Public Relations, Biotechnology and Pharmaceutical, Engineering, Finance/Economics, Information Technology, Sales, Science, Executive Management, Quality Control, Medical |
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Associate Director, Clinical Trial Patient Safety
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 atwww.abbvie.com. Follow @abbvie onLinkedIn,Facebook,Instagram,XandYouTube.
Job Description
Purpose :
This position supports the case processing organization to achieve its mission of improving patient lives
globally through industry leading safety and compliance by consistent and accurate delivery of high quality,
relevant and timely adverse event information. Responsibilities : - Directs, influences, implements and communicates case processing and reporting policy and direction for Global Product Safety.
- Evaluates new regulations and guidelines, develops plans and processes for implementation
- Communicates and coordinates across functional and global boundaries to ensure timely completion of AE cases for regulatory submission.
- Identifies, evaluates, develops and implements Global Products Safety policies, processes and system improvements.
- Manages department budgets and projects future financial and resource needs
- Identifies and anticipates potential department problems impacting the ability to meet regulatory requirements and business goals, develops and implements methods of improvement and resolution.
- Manages the audit process, prepares responses and develops associated improvement plans (e.g. FDA meetings; responses to warning letters)
- Works cross-divisionally to influence business processes which impact product safety.
- Ensures a positive employee relationship, work expectations and employee accountability.
- Strategically develops responses to employee relationship trends
- In absence of Associate Director, is responsible for Associate Director duties, including day to day activities.
Qualifications
- Bachelors degree with related health sciences background, licensed healthcare professional required. RN, BSN, BS, BS Pharm, PharmD or advanced degree preferred. Candidates lacking the appropriate degree but with equivalent previous management or leadership experience may be considered.
- Minimum 1 year clinical experience
- 4 years of pharmacovigilance experience required.
- Global exposure preferred
- Demonstrated experience in a management capacity required
- Significant experience leading cross-functional teams on complex projects required.
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 posting based on the job grade for this position.Individualcompensation paid within this range will depend on many factors including geographic location, andwemay ultimatelypay more or less than the posted range. This range may be modified in 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 to participate in 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 employee remains in the Company's sole andabsolutediscretion unless and until paid andmay be modified at 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, visithttps://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
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