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Роль чётко сосредоточена на управлении кросс-функциональными проектами в клинической геномике и работе с регулируемыми данными и диагностикой; высокие требования к опыту могут сузить круг подходящих специалистов.
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Понятная зона ответственности
Перспективная специализация
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Описание вакансии
Текст:
Hirify AI/Оригинал
TL;DR
Clinical Development Project Manager (Genomics): Leading clinical development projects from initiation through implementation and closeout, coordinating bioinformatics, software engineering, clinical operations, and product stakeholders with an accent on scalable genomic analysis, data pipelines, validation, and regulatory compliance. Focus on managing dependencies and risks, translating analytical requirements into deliverables, and driving data-informed decisions across technically complex workstreams.
Location: Remote, United States; occasional travel to conferences, partner sites, healthcare institutions, or company meetings may be required.
Company
hirify.global develops and operates clinical genetics and genomic diagnostic solutions.
What you will do
Lead Clinical Development projects from initiation through implementation and closeout, ensuring milestones, scope, quality, and timelines are maintained.
Create and manage project plans, dependency maps, risk registers, and delivery metrics across dry lab workflows.
Translate complex analytical and computational requirements into executable deliverables supporting scalable and compliant genomic analysis and reporting.
Report project status, risks, outcomes, and validation readiness to program leadership through data-driven updates.
Support regulatory, quality, data-governance, documentation, audit, and validation activities.
Requirements
Bachelor’s degree in Life Sciences, Genetics, Molecular Biology, Public Health, Healthcare Administration, Clinical Research, or a related field; an equivalent combination of education and experience may be considered.
At least 4 years of relevant experience in clinical lab operations, development and research, diagnostics, biotechnology, healthcare, or related fields, including at least 2 years managing cross-functional projects with accountability for timelines and deliverables.
Experience managing multiple technically complex projects and cross-functional teams that include bioinformatics scientists, software engineers, analysts, and clinical stakeholders.
Experience with data pipelines, analytical workflows, or laboratory informatics platforms.
Strong understanding of technical dependencies, system integrations, and validation considerations in regulated environments.
Ability to lead through ambiguity, evolving technical requirements, and data-driven decision-making, and to collaborate with technical and non-technical stakeholders at all levels.
Strong analytical, problem-solving, risk-mitigation, attention-to-detail, data-accuracy, and process-rigor skills.
Commitment to continuous improvement and operational excellence.
Nice to have
Master’s degree in life science or a related field.
Project management certification such as PMP or equivalent.
Culture & Benefits
Full-time remote work arrangement.
Work in a matrixed environment with internal clinical development and operations teams, external cross-functional groups, investigators, healthcare institutions, and strategic partners.
Occasional travel may be required for conferences, partner sites, healthcare institutions, or company meetings.
Inclusive equal-opportunity workplace with reasonable accommodations available during the application process.
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