1 день назад
Senior Director, Scientific Affairs
175 000 - 240 000$
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Senior Director, Scientific Affairs (Clinical Trials and Regulatory Laboratory Science): Providing strategic scientific leadership for clinical-trial laboratory services and R&D teams with an accent on scientific rigor, regulatory compliance, and emerging biomarkers and technologies. Focus on leading global scientific teams, validating methodologies, resolving audit findings, and expanding safety and non-safety testing capabilities.
Location: Rochester, New York, United States; relocation package available.
Salary: $175,000–$240,000 per year.
Company
provides laboratory and scientific services supporting clinical trials, safety testing, and regulatory requirements.
What you will do
- Partner with Clinical Operations leadership to define and operationalize scientific strategy.
- Lead scientific teams, manage resources, prioritize work, and monitor performance metrics.
- Oversee Principal Scientists and R&D teams supporting laboratory validation, safety testing, and expanded service offerings.
- Drive initiatives involving biomarkers, emerging technologies, scientific solutions, and process improvement.
- Serve as a scientific escalation point for internal teams, clients, 3PL partners, and regulatory stakeholders.
- Oversee audit findings, regulatory initiatives, external scientific engagement, and conference strategy.
Requirements
- PhD with 10 years of experience in a clinical-trials regulatory laboratory, or a BS in Life Sciences with 15 years of relevant experience.
- At least 5 years of progressive leadership experience.
- Experience leading teams, projects, troubleshooting, and scientific operations.
- Knowledge of clinical-trial laboratory validation and regulatory environments.
- Ability to work onsite in Rochester, New York.
Nice to have
- New York State Certification of Qualification in Clinical Chemistry, Diagnostic Immunology, Endocrinology, and/or Hematology.
- Understanding of GCP, GLP, GCLP, CAP, NYSH, and UK EMEA requirements.
- Board certification through a relevant professional certification body.
Culture & Benefits
- Full-time schedule of 40 hours per week, Monday through Friday during daytime hours.
- Relocation package available.
- Opportunities to support continuing education, coaching, mentorship, and professional development.
- Sedentary work with occasional walking or standing; reasonable accommodations are considered.
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