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Senior Medical Coder

10 Feb. 17, 2025
Job Description
Job Type: Full Time 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: Senior Medical Coder
Location: Remote, London, United Kingdom, and Geneva, Switzerland
Job Type: Part-time
Posted: Nov. 20, 2024
Job ID: 199

Job Overview:

As a Senior Medical Coder, you will be responsible for providing clinical coding support across various therapeutic areas while ensuring high-quality, accurate, and timely coding deliverables. This role also requires adherence to SOPs and maintaining audit-ready documentation, playing a critical role in coding medical terms and medications using industry-standard and company-specific conventions.

Responsibilities:

  • Adhere to SOPs and ensure documentation is audit-ready.

  • Provide coding support across multiple therapeutic areas.

  • Develop and maintain coding conventions for specific protocols or programs.

  • Perform accurate coding using industry-wide and company standards.

  • Review coded terms for accuracy and consistency, addressing discrepancies.

  • Issue queries in EDC systems to maintain high coding quality.

  • Perform impact analysis of updates to MedDRA and WHO Drug dictionaries.

  • Collaborate with internal and external clients.

  • Stay updated on current coding techniques and assist with implementing new ones.

Qualifications:

  • Education: Bachelor’s degree in Life Sciences, Computer Science, or a related field.

  • Experience: 1-2 years of experience in Clinical Data Management (coding group) or Clinical Research.

  • Skills:

    • Proficiency with coding tools (e.g., Medidata Rave Coder, Merative Zelta Coder).

    • Familiarity with MedDRA and WHO Drug dictionaries.

    • Experience in clinical trials or the pharmaceutical environment is preferred.

    • Knowledge of the clinical drug development process and relevant documents (SOPs, Guidelines).

    • Understanding of ICH-GCP and regulatory requirements such as 21 CFR Part 11.

    • Proficiency in Microsoft Office Suite (Excel, Word, PowerPoint).

    • Strong communication skills (verbal and written).

    • Detail-oriented, proactive, and able to work both independently and as part of a team.

Additional Information:

  • Location: Remote, with the option to work from London or Geneva.

  • Cytel offers a supportive work environment and encourages professional development and growth.

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