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11 дней назад

Clinical Data & Biometrics Associate Consultant (AI)

120 000 - 137 000$
Формат работы
hybrid
Тип работы
fulltime
Грейд
middle
Английский
c1
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
Clinical Data & Biometrics Associate Consultant (AI/Clinical Trials): Leading clinical data and biometrics transformation initiatives across Phase I–IV trials, with an accent on clinical data flows, submission-ready datasets, and AI-enabled analytics. Focus on designing data transformation pipelines, optimizing clinical data review and statistical programming, and bridging technical analytics with pharmaceutical and CRO stakeholders.

Location: Chicago, Illinois, United States. Hybrid working model with work-from-home and on-site presence at client or hirify.global offices; travel is required for client-facing work.

Salary: $120,000–$137,000 per year, with potential COLA, bonus incentives, and relocation benefits.

Company

hirify.global is a management consulting and technology firm that combines data, science, technology, and human ingenuity to develop solutions for life sciences and other clients.

What you will do

  • Lead or co-lead workstreams, managing timelines, deliverables, requirements, and project quality.
  • Drive clinical data and biometrics transformation initiatives for pharmaceutical sponsors and CROs.
  • Support Phase I–IV clinical trials across data collection, management, transformation, analysis, and submission.
  • Analyze clinical data flows, EDC and non-EDC systems, and standards including CDISC SDTM and ADaM.
  • Design, specify, or oversee pipelines that transform source data into submission-ready datasets.
  • Develop AI-focused programs for data review automation, anomaly detection, edit-check optimization, programming productivity, and documentation generation.

Requirements

  • Bachelor’s or master’s degree in a scientific, analytical, or technical discipline; a PhD may substitute for work experience.
  • 3–5 years of relevant experience in clinical data management, statistical programming, biometrics, or related clinical development functions.
  • Direct hands-on experience supporting human Phase I–IV clinical trials within a pharmaceutical sponsor, biotechnology company, or CRO.
  • Experience with clinical trial datasets, including EDC systems such as Medidata Rave or Veeva EDC and non-EDC sources.
  • Knowledge of GCP, clinical trial operations, regulatory expectations, CDISC, and SDTM.
  • Fluency in English and authorization to work in the United States without current or future employer visa sponsorship are required.

Nice to have

  • Exposure to AI, automation, or advanced analytics in R&D, clinical data management, or biometrics.
  • Experience with biological or real-world evidence datasets used in clinical analytics.

Culture & Benefits

  • Cross-functional skills development and customized learning pathways.
  • Milestone training programs aligned with career progression.
  • Internal mobility and opportunities for role expansion.
  • Comprehensive health, dental, life insurance, retirement, leave, and time-away benefits.
  • Collaborative, client-first working environment with flexible home and on-site work.

Hiring process

  • Submit an online application with a complete set of official or unofficial transcripts.

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