AbbVie: Senior Project Manager, Clinical Supply — North Chicago, IL, United States
AbbVie lists a Senior Project Manager, Clinical Supply opening in North Chicago, IL, United States. The position is listed as full-time. The job description covers quality assurance, manufacturing, risk management, supply chain.
Recruitment overview
| Organisation | AbbVie |
|---|---|
| Post / role | Senior Project Manager, Clinical Supply |
| Employment type | Full-time |
| Notification / job ID | R00152606 |
| Job location | North Chicago, IL, United States |
| Work arrangement | Remote |
| Educational qualification | Qualification references: bachelor’s degree |
| Experience required | Bachelor’s Degree required, preferably in physical science, math, engineering or pharmacy. 3 years total experience in Pharmaceucal industry preferred, but not required |
| Salary / stipend | See employer notice for pay details |
| Last date to apply | See official notice |
About AbbVie
AbbVie is a biopharmaceutical business focused on discovering and delivering medicines and related health solutions. Its employer introduction identifies immunology, oncology and neuroscience among its therapeutic areas, alongside the Allergan Aesthetics portfolio. The organisation's stated mission connects current health problems with the development of treatments for future medical needs. Its activities therefore have both scientific and product-delivery dimensions, with different functions supporting research, medicines and services within the named therapeutic and aesthetics areas.
The position and its setting
AbbVie lists Senior Project Manager, Clinical Supply in North Chicago, IL, United States, under reference R00152606. The details below separate the work described by the employer from essential conditions, preferred experience and practical preparation advice.
- Employment type: Full-time
- Employer listing date: 24 October 2026
- Brands: AbbVie
Responsibilities and work described
- Provides input to Clinical Study Teams to influence clinical protocol design to ensure most efficient ulizaon of supply chain resources
- Translates clinical study design into packaging design
- Authors the study medicaon and labeling secon of the clinical protocol
- Develops protocol specific labeling compliant with applicable global regulaons
- Idenfies, develops, communicates and tracks project melines, acvies, logiscs and milestones
- Creang appropriate protocol specific manufacturing and packaging work orders in concert with Third Party and IRT vendors, quality assurance, clinical team partners, etc. to ensure mely availability of clinical supplies
- Protocol specific clinical supplies scenario analysis, risk management and conngency planning
- Forecasts protocol specific bulk drug product requirements, including comparator agents, ancillary supplies and commodies, including overages
- Parcipates in cross funconal iniaves as drug subject maer expert
- Leads in funcon improvement iniaves
Essential requirements and candidate background
- Must have experience in one of the following areas: Drug Discovery (e.g. Process Chemistry, Analycal Chemistry), Drug Development (e.g. formulaon), Clinical Operaons (e.g. Clinical Project Management), Supply Chain (e.g. Clinical Supplies Project Management), Quality Assurance
- Proficiency: the applicaon of standard business requirements (for example SOPs, Global Regulaons, OEC,)
- Must have understanding of importance of compliance in a regulated environment and be capable of applying this knowledge to improve current processes
- Capable of represenng CDSM as parcipant in and contributor to cross funconal iniaves
- Work collaboravely across departments/funcons and interact in a tacul, professional and effecve manner
- Manage and priorize mulple tasks under ght deadlines and high pressure
- Problem solving and Project Management skills
- Communicaon skills (both wrien and oral)
Education and qualification routes
- Degree / qualification: Bachelor’s Degree required, preferably in physical science, math, engineering or pharmacy. 3 years total experience in Pharmaceucal industry preferred, but not required
Location, schedule and contract conditions
For this overseas or regional listing, confirm work authorisation and any location restrictions with the employer. The location does not establish visa sponsorship or permission to work remotely from India.
- Work arrangement: Remote
- Advertised location: North Chicago, IL, United States
Pay and application dates
A verified salary figure is not established in this article. An online estimate for another Senior Project Manager, Clinical Supply vacancy is not an offer for reference R00152606; use the employer’s own pay disclosure and recruitment communication.
A closing date is not confirmed in this article. Check the current employer page before submitting: an undated posting can change or be withdrawn.
How to apply to AbbVie
Applications follow the official employer page linked below.
Open the official AbbVie posting below and match the title and reference R00152606.
Compare your qualifications and experience with the essential conditions for the North Chicago, IL, United States position, then read the preferred criteria separately.
Prepare an accurate CV and the supporting items requested in that employer’s application. Provide only information and documents you are authorised to share.
Use the employer’s application option, complete the required fields and review the submission. Retain the acknowledgement when one is provided. Job Alerts World does not receive the application.
Practical preparation: quality assurance
For quality assurance, explain the process, controls and records you worked with. A useful example shows how an issue was prevented, investigated or corrected and how the change was checked.
Relevant skills
- quality assurance
- manufacturing
- risk management
- supply chain
- chemistry
- pharmacy
- compliance
- project management
Important links
| Official notification / job description | Open official page |
|---|---|
| Online application portal | Open official page |
Read the complete official notice before applying. Availability and requirements can change.
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