Associate, Support Operations l

AbbVie

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profile Job Location:

Chicago, IL - USA

profile Monthly Salary: Not Disclosed
Posted on: 30+ days ago
Vacancies: 1 Vacancy

Job Summary

Purpose

Describe the primary goals objectives or functions or outputs of this position.

Primarily responsible for the registration and accurate entry of high volumes of adverse event data into pharmacovigilance database within required timeframes to ensure compliance with departmental and regulatory guidelines.

Responsibilities

  • Accurate and timely registration of adverse event reports from initial receipt to data entry within required timeframes.
  • Accurate and timely processing of high volume of medical data within required timeframes to ensure regulatory compliance
  • Timely and accurate case prioritization for workflow routing
    Effectively prioritizes and manages own time to complete assigned tasks
  • Demonstrates functional and technical knowledge and skills to perform the job at a high level of accomplishment
  • Clearly and succinctly communicates information to customers verbally and in writing
  • Demonstrates high level of customer service to both internal and external customers
  • Utilizes judgment skills to identify issues that impact the workflow and
    uses rigorous logic and methods to solve difficult problems with effective solutions
  • Identifies gaps and areas that need improvement and communicates and/or implements recommendations/changes

Other responsibilities may include:

  • Training new personnel.
  • Performing monthly Quality Assurance checks to ensure department quality compliance.
  • Acting as Subject Matter Expert in departmental projects new system implementation or current system enhancements.
  • Performing tasks outside ones own area of responsibility to help with departmental needs.

Role Accountability/Scope includes:

  • Accountable to GCM Clinical Case Management/Support Operations management/leadership
  • staff functions with limited supervision.
  • Understands impact If errors occur which can result in compliance risk with regulatory authorities.
  • Adaptable to changing priorities.
  • Accountable for providing feedback to management/leadership on workload management.
  • Work cooperatively with cross-functional peers team members and customers.
  • Ability to deal with high-volume workflow.
  • Self-motivating and demonstrates initiatives in seeking process improvements taking on new responsibilities and seeking solutions during high/low workload period.
  •  Dedicated to meeting the expectations and requirements of internal and external customers; acts with customers/patients in mind.

This role can be remote with monthly travel to our Lake County IL headquarters. 


Qualifications :

Qualifications:
o High School Diploma required. Associate degree or Bachelors degree preferred.

Preferred experience
o 6 months to 1 year of similar work experience.
o Excellent computer and keyboarding skills including Excel PowerPoint Word and Outlook
(or equivalent email system).
o Prior experience and familiarity with computer databases.
o Superior attention to detail quality accuracy and timelines.
o Strong time management and prioritization skills; ability to multi-task.
o Strong adaptability to switching tasks to meet business needs.
o Strong customer service skills.
o Ability to work independently with minimal supervision and ability to work within a team
setting as an effective member of a team.
o Fast learner of technical and process skills/knowledge.
o Effective communications skills both verbal and written.
o Medical terminology knowledge preferred.
o Prior experience in a regulatory/medical setting preferred


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. 

  • This job is eligible to participate in our long-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 Companys sole and absolute discretion unless and until paid and may be modified at the Companys 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  & Puerto Rico applicants seeking a reasonable accommodation click here to learn more:

Work :

Yes


Employment Type :

Full-time

PurposeDescribe the primary goals objectives or functions or outputs of this position.Primarily responsible for the registration and accurate entry of high volumes of adverse event data into pharmacovigilance database within required timeframes to ensure compliance with departmental and regulatory g...
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Key Skills

  • Business
  • Information Management
  • Accounting
  • Corporate Risk Management
  • Faculty
  • Jms

About Company

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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, neuro ... View more

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