Clinical Sciences Partnership COE Coordinator

Posted 20 Days Ago
Be an Early Applicant
North Chicago, IL, USA
Hybrid
59K-104K Annually
Junior
Healthtech • Pharmaceutical
The Role
Coordinates pharmacovigilance partnership activities, including regulatory scheduling, safety inquiry routing, deliverable transfers, compliance tracking, issue investigation, metrics, reporting, training support, and stakeholder communication. Supports safety-related systems and process improvements while maintaining accuracy, quality, and compliance across partnership records and activities.
Summary Generated by Built In
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

This position reports into the Clinical Sciences Partnership CoE within the Clinical Sciences Product Office & Technology in Strategic Operations organization. The Strategic Operations organization works collaboratively and strategically with colleagues across the product lifecycle to identify, evaluate, understand and communicate the safety profile of our drugs to protect patients worldwide.

The Clinical Sciences Partnership CoE is a high-profile high-impact team that leads and owns safety decisions and strategy across the product lifecycle. The team partners with stakeholders across the product lifecycle to provide innovative safety-driven strategies, which will maximize product benefit-risk for patients. The Clinical Sciences Partnership CoE plays a critical role, working collaboratively and strategically with colleagues across AbbVie who engage with PV partners performing activities that have the potential of identifying or handling safety information related to an AbbVie product.

Responsibilities:

  • Works closely with various stakeholders to ensure scheduled activities occur per local regulation.
  • Manages multiple group mailboxes and routes safety-related inquiries to the appropriate internal and external stakeholders.
  • Collaborates with internal and external partners to coordinate the timely transfer of deliverables in accordance with PV Agreements requirements.
  • Assists in answering safety related questions for internal systems.
  • Supports development of business metrics, generates and monitors key operational metrics for performance, investigates and supports the follow-up of discrepancies.
  • Supports issue investigation, coordinates between internal and external stakeholders.
  • Supports the preparation of routine and ad hoc reports, supports the investigation of trends, and escalates issues as appropriate.
  • Supports development of materials and supports delivery of training sessions (through multiple modalities) in conjunction with supplier, including train-the-trainer, special-topics, refresher, and internal Abbie trainings as needed.
  • Supports technology systems across the Office of the PST to improve agility, effectiveness, quality and productivity of the PSTs.

 

Qualifications

  • Bachelor's Degree preferred; At least 2 years of related industry experience; pharmaceutical industry experience highly preferred.
  • Working knowledge of Pharmacovigilance processes and experience supporting partnership-related activities, including compliance tracking, deliverable coordination, and stakeholder communication.
  • Proficiency in Microsoft Office applications, including Word, Excel, PowerPoint, and Outlook, with an interest in leveraging AI-enabled and other emerging technologies to support continuous improvement and operational excellence.
  • Capable of working independently in a fast-paced environment while maintaining accuracy, compliance, and attention to detail.
  • Strong organizational and multitasking skills with the ability to manage multiple activities simultaneously and effectively prioritize competing demands.
  • Strong attention to detail and analytical skills; prior experience in a Pharmacovigilance, safety or other regulated environment preferred.
  • Demonstrates a strong quality and compliance mindset, applying effective quality control practices to ensure the accuracy, completeness, and integrity of partnership records, contractual documentation, deliverables, and related oversight activities.
  • Utilizes critical thinking skills to identify process issues and recommend practical solutions.
  • Able to organize multiple activities simultaneously to accomplish individual and departmental goals while using resources effectively and efficiently.
  • Demonstrates a commitment to continuous improvement and a willingness to adapt and enhance processes when needed.

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 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 short-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. ​

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

Skills Required

  • At least 2 years of related industry experience
  • Bachelor's degree
  • Pharmaceutical industry experience
  • Working knowledge of pharmacovigilance processes
  • Experience supporting partnership-related activities, including compliance tracking, deliverable coordination, and stakeholder communication
  • Proficiency in Microsoft Word, Excel, PowerPoint, and Outlook
  • Ability to work independently in a fast-paced environment while maintaining accuracy and compliance
  • Strong organizational and multitasking skills
  • Strong attention to detail and analytical skills
  • Experience in pharmacovigilance, safety, or another regulated environment
  • Quality and compliance mindset with effective quality control practices
  • Critical thinking and process improvement skills
  • Ability to manage multiple activities and prioritize competing demands
  • Commitment to continuous improvement and adaptability

AbbVie Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about AbbVie and has not been reviewed or approved by AbbVie.

  • Retirement Support — Retirement programs are portrayed as a standout, with a dollar‑for‑dollar 401(k) match up to 6% and an additional annual company contribution based on age and service. Feedback suggests this materially boosts perceived total compensation for many U.S. employees.
  • Parental & Family Support — Paid parental and caregiver leave are emphasized, including up to 12 weeks of fully paid parental leave for all parents and 4 weeks of paid caregiver leave in the U.S. Feedback suggests these policies are a meaningful differentiator for employees balancing family needs.
  • Leave & Time Off Breadth — Time off is described as extensive, with tiered vacation that scales with tenure, 17 company holidays, and two paid volunteer days in the U.S. Feedback suggests the breadth of leave contributes notably to overall benefits satisfaction.

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The Company
HQ: North Chicago, IL
56,000 Employees
Year Founded: 2013

What We Do

AbbVie is a global biopharmaceutical company focused on creating medicines and solutions that put impact first — for patients, communities, and our world. We aim to address complex health issues and enhance people's lives through our core therapeutic areas: immunology, oncology, neuroscience, eye care, aesthetics and other areas of unmet need.

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