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5 дней назад

Associate Director, Clinical Data Management (Biotech)

178 000 - 215 250$
Формат работы
onsite
Тип работы
fulltime
Грейд
director
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
Associate Director, Clinical Data Management (Biotech): Leading clinical data management strategy and operations for a biopharmaceutical research platform with an accent on data quality, EDC/database design, regulatory compliance, and cross-functional collaboration. Focus on designing data collection systems, resolving complex data-quality challenges, maintaining clinical data integrity, and mentoring data management teams.

Location: Jersey City, NJ or Millbrae, CA, United States

Salary: $178,000–$215,250 annually, depending on skills, competency, and market demand.

Company

hirify.global Therapeutics is a biopharmaceutical company developing novel treatments through a platform combining chemistry, engineering, computation, and biology with molecular-resolution live-cell imaging.

What you will do

  • Provide strategic leadership and operational oversight for the clinical data management function.
  • Develop data collection strategies, tools, and systems with cross-functional teams.
  • Oversee validation, discrepancy management, reconciliation, and other data quality-control activities.
  • Lead the design and maintenance of electronic data capture systems and clinical databases.
  • Ensure compliance with data standards, regulatory guidelines, and data integrity requirements.
  • Mentor data management professionals and collaborate with biostatisticians, clinical researchers, regulatory experts, and external partners.

Requirements

  • Postgraduate degree with 8+ years of relevant experience, or bachelor’s degree with 10+ years of relevant experience in life sciences, biostatistics, computer science, or a related field.
  • Extensive experience in clinical data management, including data collection, database design, and quality assurance.
  • In-depth knowledge of biotechnology or pharmaceutical clinical research practices.
  • Proficiency with data management tools, electronic data capture systems, and data coding standards.
  • Thorough knowledge of clinical data management regulations and data integrity requirements.
  • Demonstrated leadership, analytical, problem-solving, communication, and team-development skills.

Nice to have

  • Oncology experience.
  • Veeva EDC experience.

Culture & Benefits

  • 401(k) plan with company matching.
  • Medical, dental, vision, mental health, wellness, and life insurance benefits.
  • Weeklong summer and winter holiday shutdowns.
  • Generous paid time off, holiday policies, and enhanced parental leave.
  • Daily subsidized lunch program when working on-site.
  • Additional bonus and equity compensation.

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