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4 часа назад

Clinical Data Manager (Oncology)

125 000 - 175 000$
Формат работы
remote (только USA)
Тип работы
fulltime
Грейд
senior
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 Data Manager (Oncology) (Clinical Trials/CDISC): Managing high-quality clinical data across Phase 2 and Phase 1b oncology trials with an accent on data management plans, EDC systems, database builds, and regulatory compliance. Focus on overseeing CRO deliverables, cleaning and reviewing clinical data, supporting database lock and inspection readiness, and applying CDISC/SDTM standards.

Location: Remote (U.S.); eligibility to work in the United States is required.

Salary: $125,000–$175,000 per year, depending on experience, qualifications, and location.

Company

hirify.global Therapeutics is a Nasdaq-listed, clinical-stage oncology biotech company developing the PIKTOR multi-node PI3K/AKT/mTOR inhibitor program.

What you will do

  • Lead day-to-day clinical data management activities for assigned Phase 2 and Phase 1b trials.
  • Oversee CRO and external vendor deliverables, timelines, quality, and compliance.
  • Develop and review Data Management Plans, CRFs/eCRFs, edit check specifications, and data transfer specifications.
  • Manage database builds, user acceptance testing, database lock, data review, listings review, and query resolution.
  • Collaborate with clinical operations, biostatistics, medical, and vendors on data standards and analysis datasets.
  • Support GCP compliance, inspection readiness, audits, inspections, and process improvements.

Requirements

  • Bachelor’s degree in life sciences, computer science, or a related field; an advanced degree is a plus.
  • 5–8 years of clinical data management experience in biotech, pharma, or CRO settings.
  • Experience supporting Phase 1–2 clinical trials.
  • Hands-on experience with EDC systems such as Medidata Rave, Veeva, or Oracle InForm.
  • Strong understanding of CDISC and SDTM standards, GCP, and regulatory requirements.
  • Experience managing CROs and external vendors, with strong attention to detail, problem-solving, communication, and collaboration skills.

Nice to have

  • Experience with oncology trials.
  • Advanced degree in a relevant field.

Culture & Benefits

  • 100% remote work with a flexible schedule.
  • Competitive salary and equity in a well-funded clinical-stage biotech.
  • Health, dental, and vision coverage for employees and dependents.
  • Flexible time off and generous parental leave.
  • Traditional and Roth 401(k) plans.
  • Mission-oriented, remote-first culture focused on learning and meaningful impact.

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