Назад
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13 дней назад

Associate Scientific Director, Clinical Genetics

163 000 - 225 000$
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
Associate Scientific Director, Clinical Genetics (Human Genetics/Pharmacogenomics): Applying clinical genetics and pharmacogenomics expertise to late-stage research and clinical development programs with an accent on patient identification, trial design, genetic testing strategies, and clinical interpretation. Focus on designing testing approaches, interpreting large-scale genomic data, guiding reverse translational research, and integrating genetic evidence into development decisions.

Location: Cambridge, MA, United States

Salary: $163,000–$225,000 per year

Company

hirify.global is a mid-sized biotechnology company developing life-changing medicines through research and clinical development.

What you will do

  • Serve as the clinical genetics and pharmacogenomics lead across Phase I, II, and III clinical programs.
  • Advise on genetics objectives, patient identification, testing considerations, and clinical trial protocols.
  • Design genetic testing strategies, including technology, laboratory partner, vendor, and data interpretation framework selection.
  • Lead vendor procurement and address regulatory requirements for genetic data used in clinical development.
  • Interpret genetic and pharmacogenomic findings and translate them into development recommendations.
  • Lead reverse translational research supporting target validation, patient stratification, disease characterization, trial design, and treatment response.

Requirements

  • PhD, MD, PharmD, or equivalent degree in human genetics, statistical genetics, pharmacogenomics, or a related scientific or clinical field, with at least 8 years of experience.
  • At least 4 years of industry experience in human genetics, statistical genetics, pharmacogenomics, or routine clinical genetic care.
  • Strong expertise in human genetics, genomics, pharmacogenomics, genetic testing, and interpretation of large-scale genomic datasets.
  • Experience supporting late-stage research and clinical development, including clinical trial protocols and genetic testing strategies.
  • Knowledge of ethical and regulatory frameworks for human genetic data and variant interpretation and classification.
  • Experience working in matrixed multidisciplinary teams, with strong verbal and written communication skills.

Nice to have

  • Experience with genetics, genomics, biomarker, or pharmacogenomics activities in clinical trials.
  • Experience in clinical trial design and study protocol development.
  • Experience applying genomic technologies to drug discovery and development, including safety and ADME pharmacogenomics.

Culture & Benefits

  • Regular employment with short-term and long-term incentive opportunities, including bonuses and equity incentives.
  • Medical, dental, vision, life, disability, and wellness benefits.
  • Paid vacation, company holidays, personal significance days, sick time, and parental leave.
  • 401(k) program with company matching and an employee stock purchase plan.
  • Tuition reimbursement of up to $10,000 per calendar year.
  • Inclusive environment focused on collaboration, learning, growth, and belonging.

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