About this opportunity
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 at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube.
Job Description
Responsibilities:
Works closely with the ACPRU Investigational Pharmacist
Maintain accurate drug accountability: Ensures IP-related clinical trial records including the receipt, preparation, retention samples, dispensing and return of IP are maintained per USP, DEA and GCP requirements. Ensure compliance to randomization schedule for blinded studies, responsible for verification of study set up. Ensure all pharmacy materials are available and of the appropriate quality and quantity throughout the execution of every study.
Maintain accurate inventory of pharmacy supplies and ancillary supplies (e.g. rental pumps, infusion sets, IV fluids)
Assist with supporting quality audits and regulatory inspections conducted at ACPRU
Reviews SOPs, Work Instructions and Business Process documents pertaining to ACPRU pharmacy operations, including procedures concerning quality assurance, security of controlled substances, and disposal of hazardous waste and drugs
Review protocols and provide input on study-specific materials and activities that impact ACPRU workflow.
Review Dose Preparation Instructions and associated study records/templates. Including collaboration with Pharma Science and Device Development throughout all phases (0 to 4) of development at global sites.
Ensure compliance with federal and state laws, regulations, and policies governing pharmacy operations
Effectively communicates with ACPRU staff, AbbVie Management, and external vendors
Qualifications
Experience: BS in Pharmacy with 5 year; MS or equivalent with 3 years; PharmD with 1 year
Illinois Licensed Pharmacist
Demonstrated ability to learn, understand and master experimental techniques
Ability to multitask and work within aggressive timelines
Ability to focus on the future and anticipate pharmacy operation needs
Additional Information
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 roleat the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on manyfactors 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 short-term incentive programs.
Note: No amount of pay is considered to be wages or compensation until such amount isearned, vested, and determinable. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that areallocable 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 absolutediscretion, consistent with applicable 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
Job details
How this role compares
Computed from every other active Drug Discovery & Preclinical Research role in our database, not just this employer's listings.
We currently track 439 comparable Senior Drug Discovery & Preclinical Research roles across 52 biopharma companies.
Salary context
220 of 439 peers report a salary range (USD, annualized)
Peers share this role's job function and a matching or adjacent seniority level -- not necessarily the same therapeutic area or country.
Where these roles are based
Top locations among the 439 comparable roles
+ 12 more countries
Seniority mix
439 of 439 peers have a known seniority level
Therapeutic area mix
48 of 439 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden
Similar opportunities
The closest matches from our peer group, ranked by how similar they are, not how well you'd qualify for them -- treat this as market context, not a guaranteed shortlist; a weak match is labeled as one below.
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How we calculate "similar"
No black box, no LLM guesswork: a deterministic score built from four normalized attributes. Here's this role's own peer group at different match levels, so you can see the mechanism, not just the result.
Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.
0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.