Senior Specialist, Clinical Coding (Remote)

Initial Therapeutics, Inc.; Mettawa (IL); Remote; USD 60,000 - 100,000; Full time

Job summary

An established industry player is seeking a detail-oriented coding specialist to join their Global Coding Team. In this pivotal role, you will ensure the precise coding of medical data from clinical trials, contributing to significant health innovations. Your expertise in MedDRA and WHODrug will be essential as you collaborate with study teams and uphold coding conventions. This position offers the flexibility of remote work within the US, allowing you to thrive in a dynamic environment while making a profound impact on patient care and medical research.

Benefits

Paid time off

Medical insurance

Dental insurance

Vision insurance

401(k) plan

Short-term incentive programs

Qualifications

• Bachelor's degree with health science background or equivalent experience.
• Working knowledge of medical terminology and clinical trial data.

Responsibilities

• Primary coding resource for assigned studies and subject matter expert.
• Accurately code clinical trial data using MedDRA and WHODrug.

Skills

MedDRA

WHODrug

Clinical trial data systems

Problem-solving skills

Communication skills

Education

Bachelor's degree in health science

Tools

EDC coding tools

Job description

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 atwww.abbvie.com. Follow @abbvie onX,Facebook,Instagram,YouTube,LinkedInandTik 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

• Bachelors 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 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 ingood faith it will pay for this role at the time of this posting based on the job grade for this position. Individualcompensation paid within this range will depend on many factors including geographic location, and we may ultimatelypay 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/visioninsurance and 401(k) to eligible employees.

• This job is eligible to participate in our short-term incentive programs.

Note: No amount of payis considered to bewages 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 benefitsthat are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid andmay 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, visithttps://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