8 дней назад
Medical AD/Director, Oncology ED China
Вакансия из Hirify Global, списка международных tech-компанийДля мэтча и отклика нужен Plus
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Medical AD/Director, Oncology ED China (Oncology): Developing and conducting early oncology clinical studies within global compound development programs with an accent on solid tumors, biomarkers, clinical safety, and efficacy. Focus on designing protocols, leading medical review and study execution, interpreting data, managing regulatory responses, and collaborating across clinical, translational, biomarker, and drug discovery functions.
Location: Shanghai, China. The role also supports locations in Beijing, China and Shanghai, China.
Company
Johnson & Johnson MedTech develops healthcare solutions and medicines aimed at preventing, treating, and curing complex diseases.
What you will do
- Design and conduct early oncology clinical studies within global compound development programs, with a strong focus on solid tumors.
- Assess clinical safety and efficacy data and develop clinical study reports, clinical sections of INDs, and Investigator Brochures.
- Serve as Study Responsible Physician for complex local studies, creating medical review plans and making medical decisions from study initiation through closeout.
- Direct study execution, including startup, data cleaning, medical review, database lock, and responses to health authorities.
- Collaborate with discovery, translational and biomarker scientists, toxicologists, clinical pharmacologists, drug safety specialists, clinical operations, marketing, investigators, and alliance partners.
- Mentor junior colleagues, provide matrix supervision, and influence clinical development strategy.
Requirements
- MD degree required; an advanced degree such as a PhD is a plus.
- At least 2 years of oncology clinical research experience in pharmaceutical clinical development, academia, or a large regional hospital.
- Knowledge of Good Clinical Practices and regulatory requirements for high-quality oncology trials.
- Experience with protocol development, medical review, study oversight, trial execution, data quality, safety, early-phase studies, and translational endpoints.
- Working knowledge of Microsoft Excel and Word.
- Fluent written and spoken English with excellent communication skills required.
Nice to have
- PhD or another advanced degree.
- Experience with pathology diagnosis and signing primary or peer-review pathology reports.
Culture & Benefits
- Work in a matrix team supporting global clinical development programs.
- Collaborate across international scientific, clinical, operational, and commercial functions.
- Contribute to patient-focused oncology research and development.
- Apply Johnson & Johnson’s Credo and Leadership Imperatives in team goals and decision-making.
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