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7 дней назад

Medical Coder (Clinical Trials)

80 000 - 105 000$
Формат работы
remote (Global)
Тип работы
fulltime
Грейд
senior
Английский
b2
Страна
US
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Описание вакансии

Текст:
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TL;DR
Medical Coder (Clinical Trials) (MedDRA/WHODrug): Managing medical coding and serious adverse event reconciliation for clinical trials with an accent on coding accuracy, regulatory compliance, and collaboration with sponsors and clinical data teams. Focus on maintaining coding guidelines and SAE plans, resolving cross-system discrepancies, and testing coding tools within the elluminate Clinical Data Cloud.

Location: Remote

Salary: $80,000–$105,000 USD per year

Company

hirify.global provides clinical data services and the elluminate Clinical Data Cloud to help life sciences organizations manage clinical trial data, analytics, and digital trials.

What you will do

  • Design and maintain Medical Coding Guidelines and Serious Adverse Event reconciliation plans with sponsors.
  • Perform medical coding using MedDRA and WHODrug dictionaries, including coded-term and synonym-list reviews.
  • Reconcile serious adverse events across clinical trial databases, safety systems, and other sources.
  • Generate coding and SAE queries, document coding decisions, and resolve discrepancies with safety, clinical, and data management teams.
  • Support coding-tool maintenance, including UAT script creation, execution, testing, and deployment of coding and SAE listings in elluminate.
  • Participate in dictionary versioning workflows and ensure compliance with quality standards, regulations, and industry guidelines.

Requirements

  • Bachelor’s degree in a relevant health science or a professional qualification in a relevant scientific or technical discipline preferred.
  • 5+ years of experience in the pharmaceutical or biotechnology industry with medical coding experience.
  • Experience with MedDRA and WHODrug preferred.
  • Strong knowledge of ICH/GCP guidelines, 21 CFR Part 11, clinical trial methodology, and regulatory requirements.
  • Excellent verbal and written communication skills with strong attention to detail, prioritization, planning, and organization.
  • Ability to work independently and collaboratively in a team environment.

Culture & Benefits

  • Remote work environment.
  • People-first, inclusive culture focused on diversity and individual contribution.
  • Opportunities to learn, grow, and continuously improve.
  • Recognition for remote work, company vision, culture, and work-life balance.

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