data analysisproject managementdata managementsharepointclinical researchimmunologyclinical trialsscientific writingvaccinology
Вакансия из Hirify Global, списка международных tech-компаний Для мэтча и отклика нужен Plus
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Зарплата и рынок
Средняя
$150к-165к/год
$130к$150кмедиана$180к
По похожим ролям (50) ~ $150к/год
На СНГ рынке: $2.4к/мес ($1.6к - $3к)
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Средняя вакансия
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Роль дает серьезную научную ответственность в исследованиях вакцин при NIH, но сочетание руководства командой, научной экспертизы, координации данных и улучшения процессов может привести к высокой нагрузке.
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Широкий круг задачИсследования NIHОбязателен PhD
Оценка от Hirify AI
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
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Описание вакансии
Текст:
Hirify AI/Оригинал
TL;DR
Scientific Project Manager (Clinical Research): Leading clinical-trial data analysis, scientific writing, and project coordination for vaccine and monoclonal-antibody research with an accent on immunology, vaccinology, data management, and scientific rigor. Focus on coordinating multidisciplinary teams, reviewing clinical-trial analyses and protocols, managing assay-development dependencies, and improving scientific workflows and deliverables.
Location: Rockville, MD; supporting the National Institute of Allergy and Infectious Diseases at the National Institutes of Health in Bethesda, MD.
Base compensation: $150,000–$165,000 USD annually.
Company
hirify.global is a bioscience and information technology company developing translational research, biomedical informatics, and data science applications for research centers and healthcare organizations.
What you will do
Serve as Team Lead for the VRC CTP Data Analysis and Scientific Writing team, providing scientific and technical leadership, mentorship, training, and coordination.
Coordinate clinical-trial data analysis, scientific writing, deliverables, milestones, dependencies, risks, resources, and schedules.
Review clinical-trial analyses, endpoints, results, publications, presentations, protocols, analytical plans, and data-management documentation for scientific rigor and accuracy.
Provide subject-matter expertise in immunology, vaccinology, translational research, and clinical evaluation of vaccines and monoclonal antibodies.
Coordinate scientific protocol reviews, assay-development tracking, sample and data sharing, audits, workshops, and cross-functional issue resolution.
Background in miscellaneous biology, multidisciplinary science, or general science.
Experience applying clinical-trial data analysis, data-management workflows, interpretation of clinical research findings, and scientific writing practices.
Knowledge of immunology, vaccinology, translational research, clinical research, and evaluation of vaccines or monoclonal antibodies.
Ability to coordinate multidisciplinary clinical, laboratory, statistical, data-management, regulatory, and operational personnel.
Ability to review scientific and analytical deliverables, protocols, endpoints, sampling strategies, analytical plans, and statistical analysis plans.
Skills in scientific writing and communication, project management, website content management, data analysis, and graphing.
Experience with medical and scientific databases, desktop publishing and office tools, graphing and bibliographic software, MS Office, and SharePoint.
Culture & Benefits
Full medical, dental, and vision coverage for employees.
Paid time off and paid holidays.
401(k) match of up to 5%.
Educational benefits for career growth and an employee referral bonus.
Healthcare, parking, dependent-care, and transportation flexible spending accounts.
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