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Scientific Project Manager (Clinical Research)

150 000 - 165 000$
Формат работы
onsite
Тип работы
fulltime
Грейд
lead
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
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.
  • Develop reports, procedures, project-management documentation, educational materials, strategic improvements, and scientific communications.

Requirements

  • Ph.D. required.
  • 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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