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1 день назад

Sr Clinical Development Scientist (CAR-T Therapy)

Формат работы
onsite
Тип работы
fulltime
Грейд
senior
Английский
b2
Страна
UK/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
Sr Clinical Development Scientist (CAR-T Therapy): Supporting late-stage oncology clinical development and ongoing clinical trial programs with an accent on study design, protocol development, data analysis, and regulatory filings. Focus on developing clinical trial documents, interpreting scientific data, addressing procedural issues, and supporting studies in CAR-T therapy and oncology.

Location: London, United Kingdom

Company

hirify.global is a biopharmaceutical company developing cancer immunotherapies, including CAR and TCR-engineered cell therapies designed to help the immune system recognize and eliminate tumors.

What you will do

  • Support late-stage oncology clinical development in collaboration with the Clinical Scientist Program Lead.
  • Contribute to clinical study start-up, execution, close-out, and program implementation activities.
  • Develop study concept sheets, protocols, amendments, study manuals, and Investigator meeting materials.
  • Support the design of case report forms, data management manuals, and data analysis plans.
  • Review data listings, summary tables, study results, manuscripts, scientific presentations, and regulatory documents.
  • Address scientific and procedural questions, anticipate study obstacles, coordinate teams, and provide clinical monitoring when required.

Requirements

  • PharmD or PhD in clinical research or clinical pharmacology with scientific or drug development experience, or an MS with 6+ years or BS/RN with 8+ years of relevant experience.
  • Experience in biopharmaceutical, healthcare, consulting, academic, or related environments.
  • Understanding of drug development phases and clinical trials across phases.
  • Knowledge of FDA and EMA regulations, ICH guidelines, Good Clinical Practice, and standard clinical procedures.
  • Strong analytical, communication, organizational, learning, flexibility, and adaptability skills.
  • Experience with Microsoft Office and other job-related programs.

Nice to have

  • Experience with multiple myeloma or CAR-T therapy.

Culture & Benefits

  • Full-time employment.
  • Work in a mission-driven biopharmaceutical environment focused on cancer therapies.
  • Inclusive culture focused on employee development, empowerment, and strong people leadership.
  • Work according to regulatory requirements, industry Good Clinical Practice standards, and Gilead standard operating procedures.

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