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    Coding Specialist I

    Fortrea
    4+ years
    Not Disclosed
    Bangalore
    10 Nov. 6, 2024
    Job Description
    Job Type: Full Time Remote Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

    Job Title: Clinical Medical Data Coder
    Company: Fortrea
    Location: Remote
    #LI-Remote

    About Fortrea:

    Fortrea is a global leader in contract research, committed to scientific rigor and clinical development excellence. We offer comprehensive clinical development, patient access, and technology solutions across more than 20 therapeutic areas. With operations in over 90 countries, we are transforming drug and device development for partners and patients worldwide.

    Position Overview:

    We are seeking a Clinical Medical Data Coder to join our team and support the clinical data coding aspects of assigned projects. This role will involve working under supervision to manage medical data coding activities and ensure data quality, while contributing to the development of coding processes and solutions. If you are looking to grow in a collaborative environment and have a passion for medical coding and clinical trials, this could be an ideal opportunity for you.

    Key Responsibilities:

    Data Coding & Project Support:

    • Perform Clinical Data Coding: Assist with the coding of clinical medical data on assigned projects, working with supervision.
    • Collaborate with Teams: Work closely with the Coding team and Lead Data Reviewer to address all coding aspects for projects, including start-up, maintenance, and completion phases.
    • Coding Status & Liaison Support: Provide updates on coding status to project liaisons and assist in resolving any coding-related issues.

    Project & Process Management:

    • Data Management Plan Support: Assist in reviewing Data Management Plans, particularly coding-related sections, and Study-Specific Dictionary Coding Conventions.
    • Data Handling & Quality: Support the setup, maintenance, and closure of data management processes for quality coding of clinical data.
    • Process Improvement: Contribute solutions for process and efficiency improvement on coding-related tasks and projects.

    Training & Development:

    • Professional Development: Participate in internal and external training seminars to maintain coding competencies.
    • Team Collaboration: Support project staff globally to ensure client satisfaction by delivering quality coded data on time and within budget.

    Additional Responsibilities:

    • Dictionary Verification Support: Assist with dictionary verification tasks as needed.
    • Other Duties: Perform other duties as assigned, contributing to the overall success of the project and team.

    Qualifications:

    Education & Experience:

    • Required:
      • University/College degree in Life Sciences, Health Sciences, Information Technology, or a related field, or a certification in allied health professions from an accredited institution.
      • Fortrea may consider relevant equivalent experience in lieu of formal education.
    • Required Experience:
      • A minimum of 4 years of relevant experience in data management within a clinical trial setting.
      • Basic knowledge of medical coding processes and various coding tools (e.g., Medidata Coder, Central Coding).
      • Familiarity with clinical trial processes, data management, biometrics, and systems applications to support operations.

    Skills:

    • Communication Skills: Excellent oral and written communication and presentation skills.
    • Interpersonal Skills: Strong interpersonal skills with the ability to work collaboratively in cross-functional teams.
    • Knowledge of Clinical Trials: Understanding of clinical trial processes, data management, and related activities.

    What You Will Get:

    • Competitive Salary & Benefits:
      • Health, Dental, and Vision insurance
      • Life insurance, Short-Term/Long-Term Disability (STD/LTD)
      • 401(K) retirement plan
      • Paid time off (PTO) or flexible time off (FTO)
      • Employee Stock Purchase Plan (ESPP)
      • Company bonus (where applicable)

    Why Fortrea?

    At Fortrea, we value innovation and collaboration. As a Clinical Medical Data Coder, you'll have the opportunity to contribute to the success of clinical trials, ensuring data quality while working with cutting-edge technologies and methodologies. Join us as we continue to advance clinical research globally and deliver life-changing therapies to patients in need.

    Fortrea is an Equal Opportunity Employer:
    We are committed to creating a diverse and inclusive workforce and do not tolerate discrimination of any kind. We make employment decisions based on the qualifications of the individual and the needs of our business.

    Application Deadline:
    Applications will be accepted on a rolling basis until the position is filled.

    For more information about how we collect and store your personal data, please review our Privacy Statement.

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