7 дней назад
Clinical Development Coordinator (Clinical Genomics)
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
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
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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