Вакансия из Hirify Global, списка международных tech-компаний Для мэтча и отклика нужен Plus
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Зарплата и рынок
Очень мало
$104к-145к/год
$150к$170кмедиана$190к
По похожим ролям (50) ~ $170к/год
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В Company hidden четко описана роль в значимых биомедицинских исследованиях, но зарплата заметно ниже рыночного ориентира, а работа проходит на двух площадках, что может снизить привлекательность предложения.
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Ниже рынкаДве площадкиПодробное описаниеЧеткая зона ответственностиПередовые исследования
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Описание вакансии
Текст:
Hirify AI/Оригинал
TL;DR
Clinical Research Program Manager (Clinical Research): Leading the operations of multiple clinical studies in inflammatory and autoimmune diseases, connecting patient-oriented research with genomic, immunologic, microbiome, metabolomic, single-cell, spatial, and computational research with an accent on study execution, biospecimen workflows, and data quality. Focus on designing human subjects research protocols, supervising clinical research staff, coordinating regulatory submissions, and integrating clinical cohorts with molecular and computational analyses.
Location: Cambridge, Massachusetts, with work across the hirify.global and Massachusetts General Hospital
Salary: $104,000–$145,333 per year
Company
hirify.global of MIT and Harvard conducts multidisciplinary biomedical research aimed at understanding disease mechanisms and translating genetic discoveries into new therapeutics.
What you will do
Manage day-to-day operations for multiple clinical studies focused on inflammatory and immune-mediated conditions.
Design, initiate, and implement human subjects research protocols and safety monitoring plans with principal investigators and multidisciplinary teams.
Supervise, train, and support clinical research staff, including patient recruitment, medical-record abstraction, biospecimen collection, and data-quality activities.
Coordinate study start-up, regulatory submissions, Institutional Review Board materials, operational documentation, project plans, milestones, risks, and budgets.
Oversee clinical research databases, data workflows, biospecimen processing and transfer, and approved sharing with collaborators.
Connect clinical cohorts and biospecimens with genomic, transcriptomic, immunologic, microbiome, metabolomic, single-cell, spatial, and computational research.
Requirements
Bachelor’s degree in a related field with 7+ years of experience, or a master’s degree in public health, biology, or clinical research with 5+ years of relevant experience.
At least 2 years of experience training and supervising clinical research staff.
Strong strategic planning, project and program management skills, including leadership of complex studies from initiation through execution.
Experience configuring and managing complex clinical research databases and preparing data subsets for clinical researchers.
Experience leading multi-study programs across clinical, scientific, computational, and administrative teams while managing timelines, budgets, risks, and dependencies.
Excellent written, verbal, analytical, problem-solving, organizational, and interpersonal skills.
Nice to have
Experience with investigator-initiated trials.
Experience with REDCap clinical research databases.
PMP training or certification.
Culture & Benefits
Highly collaborative environment involving investigators, clinicians, research staff, computational researchers, and institutional teams.
Medical, dental, vision, life, and disability insurance.
401(k) retirement plan, flexible spending and health savings accounts.
Paid holidays, winter closure, paid time off, parental and family care leave, and an employee assistance program.
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