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2 дня назад

Clinical Scientist Associate Director (Early Development Inflammation)

192 597 - 260 572$
Формат работы
remote (только USA)
Тип работы
fulltime
Грейд
director
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
Clinical Scientist Associate Director (Early Development Inflammation) (Clinical Development): Supporting early-phase inflammation clinical trials through protocol development, study start-up, data review, and cross-functional coordination with an accent on data quality, regulatory documentation, and decision-ready clinical outputs. Focus on implementing data management plans, reviewing clinical trial data, coordinating collaborators and CROs, and supporting regulatory submissions.

Location: United States - Remote

Salary: $192,597.25–$260,572.75 annually

Company

hirify.global is a biotechnology company developing medicines across oncology, inflammation, general medicine, and rare disease.

What you will do

  • Support the setup and execution of early-phase clinical trials in inflammation with a focus on data quality.
  • Contribute to clinical protocols, Investigator Brochures, study concept documents, and other regulatory materials.
  • Provide input on data management plans, CRF design, data review, analysis, and clinical data presentations.
  • Coordinate with cross-functional study teams, clinical leadership, collaborators, consultants, and CROs.
  • Anticipate and manage issues across teams while supporting training, recruitment, and development of matrix resources.

Requirements

  • Doctorate degree and 3 years of clinical development experience; or master’s degree and 5 years; bachelor’s degree and 7 years; associate’s degree and 12 years; or high school diploma/GED and 14 years.
  • Experience supporting early- or late-phase clinical development in a relevant therapeutic area or disease indication.
  • Experience designing, monitoring, and implementing clinical trials in compliance with Good Clinical Practice and applicable regulations.
  • Knowledge of data cleaning, database lock, data extraction, clinical data outputs, and clinical data analysis tools such as Spotfire.
  • Experience contributing to regulatory submission documents, clinical regulatory responses, scientific publications, or conference presentations.
  • Strong written, oral, communication, and presentation skills for scientific and clinical data discussions.

Culture & Benefits

  • Collaborative, innovative, and science-based work environment.
  • Health, dental, vision, life, disability, and flexible spending benefits.
  • Retirement and savings plan with company contributions.
  • Annual bonus program and stock-based long-term incentives.
  • Paid time off and career development opportunities.

Hiring process

  • Applications remain open until a sufficient number of candidates are received or a candidate is selected.
  • Sponsorship is not guaranteed.

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