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Coding Specialist II

Key Facts

Remote From: 
Full time
Mid-level (2-5 years)
English

Other Skills

  • •
    Social Skills
  • •
    Communication
  • •
    Presentations
  • •
    Collaboration
  • •
    Problem Solving

Roles & Responsibilities

  • University/college degree in life science, pharmacy or related subject preferred
  • Fluent in English, both written and verbal
  • Minimum 5-7 years relevant work experience in clinical data coding
  • In-depth knowledge of medical coding process and various coding tools

Requirements:

  • Perform clinical medical data coding for assigned projects independently
  • Assist in identifying and implementing solutions to data management coding issues
  • Serve as project liaison and provide project specific coding status
  • Collaborate with project and specialty team members for data management aspects

Job description

Job Overview:

Assisting with the data management leadership on a large / global project, or multiple projects with responsibility for the Thesaurus Management; and technical oversight of all dictionary coding activities for the delivery of medical coded data according to Fortrea/client quality and integrity specifications, and project timelines and budgets. Develop and maintain a close liaison with project Lead Data Reviewer, core team members, and Clinical Lead Data Managers as appropriate.

    Summary of Responsibilities:

    • Perform the clinical medical data coding aspects of assigned projects on a global basis independently.
    • Work with the Manager and aide in personal career development, interpersonal skills, and achievement of competency standards.
    • Assist with the identification and implementation of solutions to project data management coding issues and concerns.
    • Serve as the project liaison including provision of project specific coding status.
    • Assist in review of Data management plan (wherever coding sections are applicable) and/or Study specific Dictionary Coding Conventions and Specifications.
    • Interact and collaborate with other project and specialty team members (clinical, programming, statistics, Clinical Data Management, drug safety, etc.) to support the set-up, maintenance, and closure of the data management aspects of the project to ensure consistent, cohesive data handling and quality of coded clinical data.
    • Assist in development and implementation of global SOPs and Work Instructions within functional area; liaise with other disciplines in the development of SOPs that impact functional area.
    • Maintain coding technical competencies via participation in internal and external training seminars.
    • Support project staff on achieving client satisfaction (internal and external) through delivery of quality medical coded data, on-time, and on-budget.
    • Assist in identifying areas for process improvement, efficiency improvement and implement solutions on assigned projects.
    • Assist with the dictionary verification of Fortrea standard dictionaries and client dictionaries in a timely manner.
    • Perform dictionary verification on assigned projects.
    • Review literature and research technologies/procedures for improving global thesaurus management practices.
    • All other duties as needed or assigned.

    Qualifications (Minimum Required):

    • University/college degree (life science, pharmacy or related subject preferred), or certification in a related allied health profession from an appropriately accredited institution (e.g., professional registered nursing certification, medical or laboratory technology).
    • Fortrea may consider relevant and equivalent experience in lieu of educational requirements.
    • Fluent in English, both written and verbal.

    Experience (Minimum Required):

    • Minimum (5-7) years relevant work experience in clinical data coding experience (MedDRA and WHODrug).
    • In-depth knowledge of medical coding process and various coding tools (e.g., Medidata Coder, Central Coding, etc.).
    • Demonstrated interpersonal skills.
    • Excellent oral and written communication and presentation skills.
    • In-depth knowledge of clinical trial process and data management, clinical operations, biometrics, quality management, and systems applications to support operations.
    • Working knowledge of the relationship and regulatory obligation of the CRO industry with pharmaceutical / biotechnological companies.
    • Broad knowledge of thesaurus management process.
    • Thorough knowledge of Standard Coding Dictionaries.
    • Knowledge of ICH Guidelines and GCP including international regulatory requirements for the conduct of clinical development programs, especially as related to medical coding of clinical data.
    • Knowledge of effective clinical data management practices.

    Preferred Qualifications Include:

    • MedDRA Certified.
    • Knowledge of Fortrea and the overall structure of the organization.
    • Thorough knowledge of Fortrea standard operating procedures and work instructions.

    Physical Demands/Work Environment:

    • Office or home-based work environment.
    • Travel Requirements: Regional % Of time:5 % Of the above that requires overnight stay: 50 Travel is primarily to where: Varies

    Learn more about our EEO & Accommodations request here.

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