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56 минут назад

Translational Medicine Scientist (Contractor), Shanghai/Beijing

Формат работы
onsite
Тип работы
fulltime
Английский
b2
Страна
China
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Описание вакансии

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TL;DR

Translational Medicine Scientist (Contractor), Shanghai/Beijing (Clinical Biomarkers/Oncology): Designing and coordinating clinical translational studies and biomarker analyses that support precision medicine and drug development decisions with an accent on pharmacodynamic biomarkers, patient selection, companion diagnostics, and proof-of-concept studies. Focus on interpreting disease biology, coordinating CROs and academic collaborators, and translating biomarker strategies from early- to late-phase clinical development.

Location: Onsite in Shanghai or Beijing, China

Company

Global biopharmaceutical company developing medicines across oncology and other therapeutic areas.

What you will do

  • Design, conduct, and coordinate clinical biomarker analyses across oncology and non-oncology development programs.
  • Support pharmacodynamic proof-of-mechanism, patient selection, stratification, and clinical proof-of-concept studies.
  • Identify and evaluate predictive biomarkers and develop clinical companion diagnostic tests.
  • Coordinate CROs, external vendors, academic collaborators, and key opinion leaders.
  • Collaborate with translational oncology, precision medicine, clinical pharmacology, development operations, clinical, statistical, and asset teams.
  • Present biomarker data, study plans, and tactics to support development decisions.

Requirements

  • PhD preferred, with postgraduate training, certification, or fellowship in medicine or drug development focused on disease biology and biomarkers.
  • Strong understanding of cancer biology, cancer genetics, immunology, and disease biology relevant to drug development.
  • Experience executing and interpreting cancer biomarker studies in clinical trials, including biomarker development, validation, and clinical application.
  • Familiarity with clinical trial design, study logistics, regulatory requirements, and oncology companion diagnostic development and approval.
  • Ability to work effectively in multidisciplinary teams with strong verbal and written communication skills.
  • Ability to manage CROs, build alliances, influence stakeholders, and resolve conflicts.

Culture & Benefits

  • Cross-functional collaboration across clinical, scientific, operational, and statistical disciplines.
  • Work with external research organizations, vendors, academic collaborators, and clinical experts.
  • Opportunity to contribute to precision medicine and clinical development programs.
  • Contractor position with full-time employment schedule.

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