Medical Director, Clinical Science Oncology

At Johnson & Johnson, we believe health is everything.

Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com

Job Function:
Discovery & Pre-Clinical/Clinical Development

Job Sub Function:
Clinical Development & Research – MD

Job Category:
Scientific/Technology

All Job Posting Locations:
Chiyoda, Tokyo, Japan

Job Description:

J&J IM R&D is a global organization and our JP team is part of the global TA ONC.

As one international team, we work closely with colleagues locate around the globe.

This role, Medical Director, will contribute to the global clinical development strategy via providing deep JP knowledge and clinical expertise of the tumor types.

You will work in a matrix team as a JP clinical leader, closely with the clinical project scientists in early and/or Late Development programs.

You represent the JP clinical matrix team in relevant global clinical meetings relating to the overall strategy and operational implementation of the clinical studies in the development plan.

You also oversee the execution of oncology clinical studies, ensuring consistency and quality, across the assigned development program.

If assigned, you will also work as the Study Responsible Physician, in collaboration with other functional disciplines, including GCO, Data Management, Statistics, Regulatory, etc to ensure flawless and integrated execution of start-up planning, oversight, and reporting of clinical studies in Oncology.

• Provide clinical leadership in JP project team to evaluate JP clinical inputs/recommendation to global clinical development strategy.

Work closely with Regulatory, Project leader, and other functions.

• Work closely with colleague clinical leaders/global medical head in TA ONC to ensure an integrated and strategic approach to flawless execution and systematic oversight of study protocol(s) in late development in close collaboration with key functional stakeholders.

• Lead the clinical part of PMDA/MHLW interactions.

Working closely with Medical Writing, responsible for the clinical related regulatory document development, ensure the strong evidence based clinical logic is in place to support company position.

Responsible for the clinical strategy alignment within TA ONC and with other function stakeholders.

• Lead the project scientists, ensuring appropriate training, mentoring, and supervision across the assigned study/studies within the clinical development program.

•Represent the clinical program to interact with clinical investigators, key opinion leaders and business partners such as for CDx ...