Senior Specialist, Clinical Coding (Remote)

Company Description

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 – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok.

Job Description

Purpose:

As part of the Global Coding Team (GCT), ensures accurate and consistent coding of medical data, including but not limited to, adverse events and medication data received from global clinical trials across all therapeutic areas.  

Responsibilities:

• Primary coding resource for assigned studies and serves as subject matter expert to study team members and other key stakeholders.
• Ability to accurately code clinical trial data using MedDRA and WHODrug in accordance with company conventions.
• Ability to effectively perform all Clinical Coding Team workflow requirements through the life of the trial.  
• Ability to support the identification of prohibited medications and/or other related exclusionary data.
• Ability to contribute to the development of and timely achievement of company projects and goals.  
• Represents the Clinical Coding Team when collaborating with study team members and/or other key stakeholders.
• Participates in the development and/or maintenance of coding conventions, Standard Operating Procedures, Guidelines and/or Work Instruction documents.
• Participates in the completion of dictionary upversioning workflow activities.
• Supports departmental and cross-functional business requirements.  

This role can be remote in the US. 

Qualifications

• Bachelor’s degree with related health science background: (e.g., RN, BSN, RPh) or equivalent experience. 
• Working knowledge medical and medication terminology.
• Working knowledge of MedDRA and WHODrug.
• Working knowledge of Clinical trial data systems and/or EDC coding tools.
• Demonstrates effec