Medical AD/Director, Oncology ED China

在 Johnson & Johnson，我们相信健康就是一切。 我们在医疗创新方面的实力使我们能够建立一个能够预防，治疗和治愈复杂疾病的世界,在这个世界中,治疗更智能，侵入性更低,并且解决方案是个性化的。 凭借我们在创新医学和医疗技术方面的专业知识,我们处于独特的地位,能够在当今的全套医疗保健解决方案中进行创新,以实现未来的突破,并对人类的健康产生深远的影响。 如需了解更多信息，请访问jnj.com

在我们的信条指引下，强生公司对全球范围内与我们共事的员工负有责任。我们提供一个包容的工作环境，在这里每个人都被视为独立的个体。在强生，我们尊重员工的多样性和尊严，并认可他们的价值。

工作职能：Discovery & Pre-Clinical/Clinical Development

作业子功能：Clinical Development & Research – MD

职位类别：People Leader

所有职位发布位置：Beijing, China, Shanghai, China

职位描述：
Associated Medical Director/Medical Director, China Early Development, Oncology

Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow.

Our Oncology team is focused on the elimination of cancer by discovering new pathways and modalities to finding treatments and cures. We lead where medicine is going and need innovators with an unwavering commitment to results.

Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.

Learn more at https://www.jnj.com/innovative-medicine

Johnson & Johnson Innovative Medicine is recruiting for a Associated Medical Director / Medical Director - Clinical Research. They will be a member of a matrix team dedicated to the implementation of clinical research studies that are part of a global compound development program, with a strong focus on solid tumor.

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Responsibilities include:

Acts as an expert within a specific disease area and a high-performing physician-scientist, familiar with clinical and/or translational research involving biomarkers.

In collaboration with global and local counterparts, designs and conducts earlier clinical studies, assesses clinical safety and efficacy data, and develops clinical study reports, clinical sections of INDs, Investigator Brochures, etc.

Interprets reports, prepares oral and written results of product research, and participates in the discussion of strategies formulated within the disease areas.

Collaborates closely with leaders from adjacent functions within Janssen Pharmaceuticals (e.g., discovery, translational, and biomarker research scientists, toxicologists, clinical pharmacologists, drug safety specialists), as well as personnel from Global Clinical Operations, Global Strategic Marketing, and other support functions.

Communicates closely with and provides indirect oversight to research groups, drug discovery teams, project clinical teams, and basic laboratory scientists.

Establishes strong working relationships and collaborations with external study investigators, key opinion leaders in drug development, and external alliance partners.

Serves as the Study Responsible Physician (SRP) for several complex, local studies and is responsible for creating the medical review plan and making medical decisions to execute assigned local study from the initiation to the closing and serves as local delegate of global SRP when support is needed.

Manages study start-up, and directs and guides study team in study execution, data cleaning, medical review, database lock, managing health authority responses, including prostate cancer–specific safety, efficacy, and benefit–risk

Executes medical-related consultation for internal stakeholders to ensure unbiased data interpretation.

May provide determination of pathology diagnosis and act as a signatory to primary and peer review pathology reports.

Strategizes and influences a goal-oriented clinical development team.

Guides junior colleagues through consultation and mentoring in techniques and processes, and provides functional (matrix) supervision.

Integrates Johnson & Johnson‘s Credo and Leadership Imperatives into team goals and decision making.

Qualifications - External

An MD is required; Advanced degree (PhD) is a plus.

A minimum of 2 years of oncology clinical research experience in clinical development within pharmaceutical industry or equivalent experience in academic or large regional hospital is required.

Knowledge of Good Clinical Practices and regulatory requirements for the conduct of high quality oncology clinical trials is required.

Experience in protocol development, medical review, oversight of study conduct, running trials, data quality and safety are strongly preferred, including early‑phase studies and translational endpoints.

Working knowledge of the use of Microsoft suite of software products including Excel and Word is required.

Fluent in written and spoken English with excellent communication skills is required.

Required Skills:

Preferred Skills:
包容性领导力, 创新, 科学评价, 科学研究, 利益相关者管理, 临床试验, 临床研究和法规, 临床运营, 领导力, 培养他人, 全球市场, 市场研究, 数据管理和信息学, 数据治理, 项目群管理, 协作, 行业分析, 研究伦理, 药物发现开发