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Director, Translational Research and Biomarkers (Genomics)

186 489 - 278 875$
Формат работы
onsite
Тип работы
fulltime
Грейд
director
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
Director, Translational Research and Biomarkers (Genomics): Leading biomarker and genomics research supporting clinical drug development, including multi-omics analysis, pharmacodynamic marker identification, and patient stratification with an accent on experimental design, clinical trial integration, and bioinformatic interpretation. Focus on managing cross-functional and external collaborations, overseeing outsourced biomarker measurement, and translating complex datasets into clinical development and regulatory decisions.

Location: Princeton, New Jersey, United States

Salary: $186,489–$278,875 per year, plus incentive opportunity.

Company

hirify.global is a pharmaceutical company developing clinical solutions through translational medicine, genomics, biomarker research, and drug development.

What you will do

  • Lead and participate in cross-functional project teams supporting clinical drug development programs.
  • Manage the selection, integration, and measurement of biomarkers in clinical trials.
  • Design biomarker and genomic research plans based on clinical data gaps and mechanistic hypotheses.
  • Oversee analysis of multi-omics and other large datasets to identify pharmacodynamic markers and enable patient stratification.
  • Manage external investigators, academic centers, vendors, and research collaborators.
  • Recommend clinical trial design elements and emerging technologies to senior leadership and support regulatory submissions when applicable.

Requirements

  • PhD or MS in Life Sciences with at least 10 years of relevant experience in clinical science, clinical research, or a related scientific field.
  • Managerial and supervisory experience.
  • Experience designing and conducting biomarker and genomics experiments and interpreting data for drug development and clinical trial design.
  • Strong knowledge of biochemical, molecular, and cellular assays, including RNA-Seq, exome and whole genome sequencing, high-throughput proteomics, and multiplex flow cytometry.
  • Experience managing multiple projects under strict deadlines and changing priorities.
  • Excellent verbal and written communication skills, including presenting complex scientific results and ideas.

Nice to have

  • Knowledge of digital biomarkers in clinical trials.
  • Proficiency in computational genomics and bioinformatic pipelines.
  • Vendor management experience covering timelines, deliverables, contracts, and regulatory compliance.
  • Experience contributing to regulatory submissions and health authority interactions.

Culture & Benefits

  • Cross-functional collaboration with internal teams, external organizations, academic centers, and investigators.
  • Medical, dental, vision, and prescription drug coverage.
  • Basic life, accidental death and dismemberment, short- and long-term disability insurance.
  • Tuition reimbursement and student loan assistance.
  • Generous 401(k) match, flexible time off, paid holidays, and paid leave programs.

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