13 дней назад
Associate Scientific Director, Clinical Genetics
163 000 - 225 000$
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
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
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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