6 дней назад
Nonclinical Toxicology Study Monitoring Scientist (AI)
101 600 - 152 400$
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Nonclinical Toxicology Study Monitoring Scientist (AI) (Nonclinical Safety/CRO Oversight): Overseeing outsourced toxicology and nonclinical safety studies for small and large molecule programs, including cell and gene therapies, with an accent on scientific rigor, GLP compliance, data quality, and CRO execution. Focus on monitoring concurrent studies, resolving operational and scientific issues, supporting regulatory documentation, and applying digital and AI-enabled solutions to improve study oversight.
Location: Boston, MA. Hybrid option allows remote work up to two days per week; on-site option requires five days per week on-site. Travel: 30%–50% for on-site study monitoring visits and vendor interactions.
Salary: $101,600–$152,400 base salary per year, plus annual bonus and equity eligibility.
Company
Vertex is a global biotechnology company focused on scientific innovation and the development of therapies for patients.
What you will do
- Provide scientific, technical, and operational oversight of outsourced nonclinical toxicology and safety studies.
- Partner with project toxicologists and cross-functional stakeholders to develop, review, and operationalize study protocols.
- Monitor CRO and partner studies through on-site visits and remote oversight, assessing study conduct, data quality, protocol compliance, and GLP adherence.
- Identify, escalate, and help resolve scientific, technical, operational, and execution issues.
- Prepare monitoring reports, visit summaries, stakeholder communications, and follow-up documentation for multiple concurrent studies.
- Support CRO qualification, vendor assessment, audit activities, regulatory documentation, and AI-enabled improvements to study oversight.
Requirements
- Master’s degree in life sciences or a related science with 3+ years of relevant experience, or bachelor’s degree with 4+ years of relevant experience.
- Hands-on in vivo laboratory experience in a CRO, pharmaceutical, or biotechnology setting.
- Experience with nonclinical safety assessment for both small and large molecule modalities, including outsourced toxicology studies.
- Working knowledge of Good Laboratory Practice regulations and sponsor oversight expectations.
- Strong scientific, organizational, problem-solving, communication, and multitasking skills in a fast-paced matrixed environment.
- Willingness and ability to travel 30%–50% and work in the Boston-based hybrid or on-site arrangement.
Nice to have
- Experience with regulatory submissions and nonclinical sections.
- Experience in vendor qualification, audit support, or CRO performance management.
- Experience using dashboards, digital tools, or AI-assisted technologies to improve study planning and oversight.
Culture & Benefits
- Continuous learning and encouragement to adopt advances in AI, technology, automation, and industry practices.
- Medical, dental, and vision benefits with paid time off and company shutdowns in summer and winter.
- Educational assistance, including student loan repayment programs.
- Commuting subsidy, matching charitable donations, 401(k), and other total rewards.
Будьте осторожны: если работодатель просит войти в их систему, используя iCloud/Google, прислать код/пароль, запустить код/ПО, не делайте этого - это мошенники. Обязательно жмите "Пожаловаться" или пишите в поддержку. Подробнее в гайде →
Похожие вакансии
11 дней назад
Director, Nonclinical Toxicology Operations
220 700 - 252 667$
10 дней назад
Associate Director, Nonclinical Program Development (Biotech)
181 000 - 214 000$
10 дней назад
Research Leader (Toxicology)
11 дней назад
Senior Scientist Bioassay Development and Quality Control (Gene Therapy)
100 500 - 145 166$
10 дней назад
Scientist I, Analytical Development (Cell and Gene Therapy)
96 267 - 126 351$
9 дней назад
Senior Scientist, Analytical Development and Quality Control - Drug Product (Biopharma)
161 100 - 185 600$