обновлено 8 дней назад
Clinical Lead Early Development and Experimental Therapeutics - Oncology
206 250 - 297 917$
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Clinical Lead Early Development and Experimental Therapeutics - Oncology (Oncology/Translational Medicine): Designing and leading early clinical development for oncology assets from first-in-human studies through phase 2a, with an accent on proof-of-mechanism, proof-of-concept, biomarker interpretation, and human target validation. Focus on dose escalation, medical safety oversight, cross-functional trial execution, CRO coordination, and translating preclinical findings into clinical studies.
Location: Cambridge, MA or Morristown, NJ; hybrid; US and Puerto Rico residents only
Salary: $206,250–$297,916.66 per year
Company
is an R&D-driven biopharmaceutical company developing medicines and vaccines through immunoscience, AI, data, and digital platforms.
What you will do
- Design and lead early clinical development studies for oncology assets, from first-in-human studies through phase 2a.
- Develop protocols covering dose escalation, proof-of-mechanism, proof-of-concept, natural history, mechanistic, and signal-seeking studies.
- Provide clinical expertise for preclinical data interpretation, translational medicine, biomarker research, and human target validation.
- Make decisions on protocol design, dose selection, study safety, and early Go/No-Go recommendations.
- Oversee medical monitoring, CROs, clinical operations, study documentation, data review, and clinical study reporting.
- Coordinate global project teams and collaborate with research, toxicology, pharmacology, regulatory, safety, biostatistics, and biomarker specialists.
Requirements
- MD or equivalent required.
- At least 3 years of clinical research experience required.
- English required.
- Experience designing or conducting early clinical trials, ideally phase 1/2a oncology studies.
- Experience with medical safety oversight, translational or biomarker research, and interpretation of preclinical data.
- Knowledge of GCP practices, cross-functional team leadership, clinical documentation, and work in a matrix organization.
Nice to have
- MD and PhD or comparable bench science experience.
- Experience with combination therapies and drugs targeting cytoplasmic signaling pathways.
- Experience using emerging digital or AI-driven tools and working in a global pharmaceutical environment.
- Postgraduate residency training, laboratory research, or late-phase clinical trial experience.
Culture & Benefits
- Work with a future-focused biopharmaceutical research organization addressing unmet needs in oncology.
- Opportunities for career growth through promotions or international and lateral moves.
- Healthcare, prevention, wellness, and family benefits, including at least 14 weeks of gender-neutral parental leave.
- Access to AI, data, and digital platforms supporting drug discovery and development.
- Collaborative work with investigators, clinical experts, regulatory authorities, CROs, and multidisciplinary internal teams.
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