3 дня назад
Clinical Science Director (Oncology)
195 000 - 277 500$
Мэтч & Сопровод
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Описание вакансии
Текст:
TL;DR
Clinical Science Director (Oncology) (clinical development): Designing and developing early- and late-phase oncology studies with an accent on clinical trial protocols, investigator collaboration, safety analysis, and regulatory documentation. Focus on interpreting clinical data, preparing scientific publications and health-authority reports, and coordinating complex studies involving targeted and immunological therapies.
Location: Alameda, California, United States, with remote work available from the United States; 10–25% travel required.
Base salary: $195,000–$277,500 annually, depending on geographic market, knowledge, skills, experience, and internal equity.
Company
is a biotechnology and pharmaceutical company developing investigational therapies, including oncology medicines.
What you will do
- Design, plan, and initiate early- and late-phase clinical oncology studies and develop study synopses, protocols, and related documentation.
- Collaborate with clinical operations and study teams on informed consent forms, case report forms, training materials, site visits, and investigator meetings.
- Work with investigators and oncology thought leaders, support investigator selection, and maintain relationships throughout clinical studies.
- Analyze and report potential safety events and contribute to clinical data interpretation, regulatory filings, and study close-out reports.
- Write and review abstracts, publications, presentations, and scientific materials for physicians, external customers, and internal stakeholders.
- Provide clinical education and feedback on emerging clinical and competitive trends in oncology.
Requirements
- Pharm.D., PhD, or M.D. with at least 8 years of related experience, or an equivalent combination of education and experience.
- 5–8 years of clinical development experience in biotechnology, pharmaceuticals, academia, or a combination of these environments.
- Experience participating in clinical oncology studies involving molecular targeted or immunological therapies.
- Detailed knowledge of clinical trial implementation and the drug development process, including the design, execution, and reporting of oncology trials with small- and large-molecule candidates.
- Strong analytical, business communication, public speaking, presentation, organizational, and problem-solving skills.
- Ability to work under tight timelines and apply sound judgment to complex clinical and scientific problems.
Culture & Benefits
- Collaborative office environment focused on sharing ideas and solutions.
- Comprehensive employee benefits, including medical, dental, vision, life, disability, and flexible spending account coverage.
- 401(k) plan with company contributions and eligibility for a discretionary annual bonus and long-term incentives.
- 15 vacation days in the first year, 17 paid holidays including a company-wide winter shutdown, and up to 10 sick days annually.
- Company-provided equipment, including dual monitors and ergonomic chairs.
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