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3 дня назад

Clinical Trial Associate, APAC (Oncology)

104 000 - 126 000$
Формат работы
hybrid
Тип работы
fulltime
Грейд
junior
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
Clinical Trial Associate, APAC (Oncology) (Clinical Operations): Supporting the planning, coordination, and execution of Phase I–III global oncology clinical studies with an accent on study documentation, site start-up, trial supplies, data quality, and regulatory compliance. Focus on coordinating investigator and monitoring activities, maintaining trial master files, tracking patient recruitment, and resolving operational issues across Asia-based trial sites.

Location: Hybrid onsite presence required at least 3 days per week in either Jersey City, New Jersey or Millbrae, California.

Salary: $104,000–$126,000 per year, depending on skills, competency, and market demand.

Company

hirify.global Therapeutics is a biopharmaceutical company developing treatments for life-threatening diseases through technologies combining chemistry, engineering, computation, and biology.

What you will do

  • Support planning, coordination, and execution of Phase I–III global oncology clinical studies.
  • Prepare and maintain protocols, informed consent forms, case report forms, trial master files, and other essential study documents.
  • Coordinate study start-up activities, including site selection, feasibility assessments, ethics committee submissions, investigator meetings, and study initiation visits.
  • Track trial supplies, investigational products, study progress, patient recruitment, enrollment, timelines, and milestones.
  • Review and resolve data queries in electronic data capture systems and support the preparation and coordination of site monitoring visits.
  • Facilitate communication among study teams, investigators, and site personnel while ensuring compliance with regulations, monitoring plans, and internal SOPs.

Requirements

  • Advanced degree with no experience, or a bachelor's degree with 2 years of relevant experience in life sciences, healthcare, or a related field.
  • Fluency in Mandarin, Cantonese, Japanese, or Korean is required.
  • Knowledge of clinical trial regulations and guidelines, including ICH-GCP and FDA requirements.
  • Experience with clinical trial management systems and electronic data capture systems.
  • Strong organization, attention to detail, communication, prioritization, and independent working skills.
  • Proficiency in Microsoft Word, Excel, PowerPoint, and Project.

Nice to have

  • Previous experience as a Clinical Trials Associate, Study Coordinator, or in a similar pharmaceutical, biotechnology, or CRO role.
  • Adaptability and willingness to learn new technologies, processes, and industry trends.

Culture & Benefits

  • Collaborative, cross-functional environment focused on advancing oncology treatments.
  • 401(k) plan with company matching.
  • Medical, dental, and vision insurance with substantial premium coverage.
  • Paid time off, holiday policies, and weeklong summer and winter shutdowns.
  • Mental health and wellness benefits, enhanced parental leave, life and AD&D insurance, and subsidized onsite lunches.

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