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1 день назад

Clinical Development Scientist (CAR-T Therapy)

133 195 - 172 370$
Формат работы
onsite
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 Development Scientist (CAR-T Therapy): Supporting late-stage oncology clinical development and ongoing clinical trial programs with an accent on protocol development, study execution, data analysis, and regulatory submissions. Focus on integrating scientific literature into new study development, addressing clinical study challenges, and supporting CAR-T and multiple myeloma research.

Location: Parsippany, New Jersey, United States; travel may be required

Salary: $133,195–$172,370 per year for other US locations; Bay Area range is $146,540–$189,640 per year. Additional bonus, stock-based incentives, paid time off, and benefits may apply.

Company

hirify.global is a biopharmaceutical company developing personalized CAR T-cell and TCR-engineered cell therapies for cancer treatment.

What you will do

  • Support late-stage oncology clinical development in collaboration with the Clinical Scientist Lead.
  • Contribute to clinical trial start-up, execution, closeout, and functional area activities.
  • Develop study concept sheets, protocols, amendments, study manuals, and Investigator meeting materials.
  • Support CRF, data management manual, data analysis plan, data listing, summary table, manuscript, and scientific presentation development.
  • Assist with regulatory document preparation and review, and address scientific and procedural questions from investigators.
  • Identify and resolve moderately complex clinical study obstacles and provide clinical monitoring when needed.

Requirements

  • Bachelor's degree with six years of experience, or a master's degree with four years of experience.
  • Relevant scientific or drug development experience and knowledge of clinical trial design and drug development phases.
  • Knowledge of FDA and EMA regulations, ICH guidelines, GCP, and standard clinical procedures.
  • Strong analytical, communication, and organizational skills, with the ability to learn quickly and adapt across projects.
  • Ability to enter a new therapeutic area, evaluate published scientific literature, and apply it to study development.
  • Proficiency with Microsoft Office and other job-related programs; ability to travel when needed.

Nice to have

  • PharmD or PhD in clinical research or clinical pharmacology.
  • Experience in multiple myeloma and/or CAR-T therapy.

Culture & Benefits

  • Focus on developing innovative cancer immunotherapies and advancing personalized cell therapies.
  • Inclusive work environment centered on employee development and empowerment.
  • Medical, dental, vision, and life insurance plans for eligible employees.
  • Paid time off, discretionary annual bonus, and potential stock-based long-term incentives.

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