Project Coordinator, Clinical Supply

AbbVie Inc.

Chicago (IL)

Hybrid

USD 55,000 - 75,000

Full time

3 days ago
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Benefits offered by this job

Comprehensive benefits package
401(k) plan

Job summary

AbbVie in the United States seeks an entry-level Clinical Supply Chain project coordinator responsible for managing documentation and simple packaging tasks in a GMP environment. You will work closely with CSPMs to ensure investigational drug supplies reach clinical sites and depots on time.

Responsibilities include planning, scheduling, coordinating packaging activities, translating requests into packaging designs, and tracking milestones.

Qualifications

  • Bachelor's Degree in physical science, math, engineering or pharmacy.
  • 0 - 2+ years total experience in the Pharmaceutical Industry.

Responsibilities

  • Planning, scheduling, coordination and execution, in support of CSPMs to ensure timely availability of investigational drug supplies and related services to clinical sites and depots.
  • Translates stability and packaging requests into an executed packaging design.
  • Identifies, develops, communicates and tracks task completion dates, activities, logistics, and milestones in support of CSPMs to ensure timely availability of investigational drug supplies.

Education

Bachelor's Degree

Job description

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, Xand YouTube.

Job Description

Serves as an individual contributor responsible for project management of key Clinical Supply Chain documentation, tasks and simple packaging activities in a GMP environment.

Responsibilities:

  • Planning, scheduling, coordination and execution, in support of CSPMs to ensure the timely availability of investigational drug supplies and related services to clinical sites and depots.
  • Translates stability and packaging requests into an executed packaging design.
  • Identifies, develops, communicates and tracks task completion dates , activities, logistics, and milestones in support of CSPMs to ensure the timely availability of investigational drug supplies .
  • Responsible for creating appropriate protocol specific manufacturing and packaging work orders in concert with the CSPM.
  • Responsible to complete, upon request of the CSPM, tasks identified for the Center of Excellence team.

Key Stakeholders:

  • The Clinical Drug Supply Chain including R43E, Analytical, Quality, and globally with our Germany counterparts as this role is key in the transfer of clinical drug to Germany from Lake County.
Qualifications
  • Education: Bachelor’s Degree required, preferably in physical science, math, engineering or pharmacy
  • 0 - 2+ years total experience in the Pharmaceutical Industry
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 thetimeofthis posting based on the job grade for this position.Individualcompensation paid within this range will depend on many factors including geographiclocation,andwemayultimatelypaymore or less than the posted range. This range may bemodifiedin 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 toparticipatein our short-term incentiveprograms.

Note: No amount of payis considered to bewages or compensation until such amount is earned, vested, anddeterminable.Theamountandavailabilityof anybonus,commission, incentive, benefits, or any other form ofcompensation and benefitsthat are allocable to a particular employeeremainsin the Company'ssoleandabsolutediscretion unless and until paid andmay bemodifiedat the Company’s 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, 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

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