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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 XFacebookInstagramYouTubeLinkedIn 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). 
  • 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 effective problem-solving and communication skills.
  • Demonstrates ability to work independently as well as in a team environment.

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, serving our community and embracing diversity and inclusion.  It is AbbVie’s policy to employ qualified persons of the greatest ability without discrimination against any employee or applicant for employment because of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information, gender identity or expression, sexual orientation, marital status, status as a protected veteran, or any other legally protected group status.

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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Average salary estimate

$95000 / YEARLY (est.)
min
max
$80000K
$110000K

If an employer mentions a salary or salary range on their job, we display it as an "Employer Estimate". If a job has no salary data, Rise displays an estimate if available.

What You Should Know About Senior Specialist, Clinical Coding (Remote), AbbVie

If you’re ready to take your coding skills to the next level, AbbVie is looking for a Senior Specialist, Clinical Coding to join our dynamic team remotely from anywhere in the U.S. In this role, you will serve as the primary coding resource for various clinical studies, ensuring that adverse events and medication data from global clinical trials are accurately and consistently coded. Your expertise in MedDRA and WHODrug will shine as you engage with study teams and key stakeholders, contributing to the development of coding conventions and maintaining compliance with internal guidelines. You’ll play a vital part in the entire trial lifecycle, participating actively in identifying prohibited medications and exclusionary data. Collaboration is key here, and you’ll represent the Clinical Coding Team while working cross-functionally to achieve project goals. Plus, with AbbVie’s commitment to innovation in therapeutic areas like immunology and oncology, this is a chance to make a meaningful impact. Candidates should have a related health science background, demonstrated problem-solving abilities, and effective communication skills. If you're passionate about enhancing people’s lives through your work, then apply today and be part of a mission that matters!

Frequently Asked Questions (FAQs) for Senior Specialist, Clinical Coding (Remote) Role at AbbVie
What are the key responsibilities of a Senior Specialist, Clinical Coding at AbbVie?

As a Senior Specialist, Clinical Coding at AbbVie, your responsibilities include acting as the primary coding resource for assigned studies, accurately coding clinical trial data using MedDRA and WHODrug, and supporting the identification of prohibited medications in clinical trials. You'll be involved in the entire clinical trial process, contributing to coding conventions and collaborating with study team members to ensure timely achievement of project goals.

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What qualifications are needed for the Senior Specialist, Clinical Coding position at AbbVie?

To qualify for the Senior Specialist, Clinical Coding position at AbbVie, candidates should have a Bachelor's degree in a related health science field, such as nursing or pharmacy. Additionally, a working knowledge of medical terminology, MedDRA, WHODrug, and clinical trial data systems is essential. Effective communication, problem-solving skills, and the ability to work independently or in a team environment are also vital.

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Is the Senior Specialist, Clinical Coding role at AbbVie remote?

Yes, the Senior Specialist, Clinical Coding role at AbbVie is a remote position, allowing you to work from anywhere in the U.S. This flexibility is part of AbbVie’s commitment to supporting their employees’ work-life balance while ensuring they contribute meaningfully to the organization's goals.

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What tools or systems will a Senior Specialist, Clinical Coding at AbbVie work with?

In the role of Senior Specialist, Clinical Coding at AbbVie, you will work with various coding and clinical trial data systems, including EDC coding tools and databases that facilitate the accurate coding of adverse events and medication data. Familiarity with MedDRA and WHODrug is critical in executing your responsibilities effectively.

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What is the impact of the Senior Specialist, Clinical Coding role on AbbVie’s mission?

The Senior Specialist, Clinical Coding at AbbVie plays a crucial role in translating clinical data into meaningful insights that drive the company's mission to deliver innovative medicines. By ensuring accurate coding, you contribute directly to the integrity of clinical trials, which is vital for advancing research in therapeutic areas like immunology, oncology, neuroscience, and eye care.

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Common Interview Questions for Senior Specialist, Clinical Coding (Remote)
Can you explain what MedDRA and WHODrug are and their relevance in clinical coding?

MedDRA and WHODrug are standardized medical terminology coding systems used for classifying adverse event reports and medication data in clinical trials. As a candidate, you should emphasize how your expertise with these systems enhances the accuracy of data management and reporting, ensuring compliance with regulatory standards.

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Describe a challenge you've faced in clinical coding and how you resolved it.

In answering this question, you should highlight a specific instance where you identified inaccuracies in coding. Discuss the steps you took to rectify the issue, such as consulting with team members for clarity, applying coding conventions, and ensuring that all historical data was updated correctly.

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How do you ensure compliance with coding guidelines in your work?

Talk about your systematic approach to staying updated with coding guidelines and conventions. Mention regular training sessions, peer review processes, and maintaining documentation that supports compliance with both internal and external standards.

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What techniques do you use to stay organized while coding large data sets?

You can discuss techniques such as developing a workflow process, using coding tools effectively, and setting priorities based on deadlines and complexity. Emphasize how staying organized helps ensure accuracy and supports timely project completion.

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How do you handle feedback regarding your coding assignments?

Explain your openness to feedback and how you view it as a tool for growth. Discuss an instance where feedback led to improvements in your scoring and coding practices, showcasing your commitment to continuous learning.

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What role does communication play in your job as a clinical coder?

Communication is vital for successful clinical coding, as you often need to clarify data with clinical teams or stakeholders. Describe your approach to keeping communication lines open, ensuring that all parties understand coding conventions and share updates transparently.

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How do you approach learning new coding technologies or systems?

Speak about your proactive attitude toward learning, whether through self-study, formal training, or collaborative learning opportunities. Highlight a recent technology or system you have successfully learned and implemented in your work.

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Can you provide an example of how you contributed to a coding convention or guideline?

Share a specific project where you collaborated with cross-functional teams to develop or refine coding conventions. Describe how your insights improved accuracy or efficiency, emphasizing the significance of teamwork in achieving project goals.

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Describe your experience with clinical trial data management systems.

Discuss specific systems you've worked with, your level of expertise, and how you used those systems to input and manage clinical data. Explain how your familiarity with these systems enhances your efficiency as a clinical coder.

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What are your career goals as a Senior Specialist, Clinical Coding at AbbVie?

Outline your aspirations to grow in this role, potentially taking on leadership responsibilities or mentoring new coders. Emphasize your commitment to AbbVie’s mission of innovation and excellence in healthcare and how you envision contributing to that goal.

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AbbVie’s mission is to discover and deliver innovative medicines 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: i...

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March 25, 2025

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