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7 дней назад

Clinical Development Coordinator (Clinical Genomics)

Формат работы
remote (только USA)/hybrid
Тип работы
fulltime
Грейд
junior
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 Development Coordinator (Clinical Genomics): Coordinating clinical development activities across genomic testing, rare disease, precision medicine, and evidence-generation programs with an accent on project tracking, documentation, and cross-functional communication. Focus on maintaining timelines, coordinating clinical studies and registries, preparing status reporting, and keeping development records audit-ready.

Location: United States; remote and hybrid work listed

Company

hirify.global develops clinical genomics and precision medicine solutions.

What you will do

  • Coordinate Clinical Development project plans, timelines, meetings, deliverables, action items, and risk escalation.
  • Support clinical studies, registries, observational initiatives, evidence-generation programs, and strategic collaborations.
  • Coordinate communication across Clinical Development, Medical Affairs, Regulatory Affairs, Laboratory Operations, R&D, Bioinformatics, Quality, Commercial, and external partners.
  • Prepare dashboards, status reports, presentations, agendas, meeting minutes, decision logs, and leadership updates.
  • Maintain complete, accurate, current, and audit-ready project and study documentation.

Requirements

  • Bachelor’s degree in Life Sciences, Genetics, Molecular Biology, Public Health, Healthcare Administration, Clinical Research, or a related field.
  • At least 2 years of experience in clinical research, clinical operations, clinical development, project coordination, biotechnology, diagnostics, pharmaceutical development, healthcare, or a related field.
  • Ability to manage multiple priorities in a deadline-driven environment and coordinate activities across stakeholders and functional teams.
  • Strong organizational, documentation, meeting coordination, project tracking, communication, and attention-to-detail skills.
  • Proficiency in Microsoft Office, including Excel, Word, PowerPoint, Outlook, Teams, and SharePoint.

Nice to have

  • Master’s degree or PhD.
  • Experience with clinical trials, registries, observational studies, or evidence-generation programs.
  • Familiarity with GCP, clinical study documentation, regulatory processes, or healthcare compliance.
  • Experience with CROs, academic medical centers, healthcare systems, industry partners, genomics, molecular diagnostics, rare disease, precision medicine, or laboratory-developed testing.
  • Experience with Smartsheet, Microsoft Project, Monday.com, Asana, or Jira.

Culture & Benefits

  • Work includes virtual and in-person meetings with internal and external stakeholders.
  • Occasional travel to conferences, partner sites, healthcare institutions, or company meetings may be required.
  • Work requires regular use of a computer workstation and review of technical, scientific, operational, and regulatory documentation.
  • Equal opportunity workplace committed to an inclusive and diverse environment.

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