Medical Affairs Manager, Neurovascular Japan

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 jnj.com . As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit. Job Function: Medical Affairs Group Job Sub Function: Medical Affairs – MD Job Category: Scientific/Technology All Job Posting Locations: Chiyoda, Tokyo, Japan Job Description:

SUMMARY:     The purpose of the position is to strategically provide medical supervision ,   support business activities,   evidence   generation /dissemination ,   educational   activities   and   engage with   internal/external stakeholders.   Leading with an outside-in vision to assimilate opportunities   identifying   market u nmet needs, this role   provides   medical/ scientific   in sights .   Additionally, this position has a role as an SRP (study responsible physician) for clinical studies.     Essential / Principal duties and responsibilities:     Medical Governance: To ensure   h ealth   c are   c ompliance on promotional material and   h ealth   c are   p rofessional   qualification   in accordance with   J&J policy, company GOP/ SOP   and related working   procedure . To ensure the contents and medical claim in   following   parts, including Indication, contraindication potential complications, clinical trial related contents, caution/ precaution   and adverse   event   are   accurate ,   fair   and objective.   SRP   (Study Responsible Physician ) :   To   be r esponsible for   performing safety review and mak ing   a recommendation about continuation or termination of clinical   trials   based on medical   expertise .   Play   a r ole   of the   s tudy safety lead   as a medical doctor.   Safety Vigilance: To work with vigilance safety members as a team to ensure that the information   regarding   a dverse   e vents in the field ,   facilitate   an accurate   and transparent communication   on   a dverse   e vents   and complaints   internally and   properly review   the m .   To a ssess device performance including clinical benefits and safety profile s. E valuate the   appropriate   r isk- b enefit   balance to support market registration and throughout   life   cycle.   MIR: To provide scientific and medical information to internal   stakeholders   and external customers, including unsolicited requests from healthcare professionals to ensure clinically   appropriate   and safe use of company products.   To c ollect   the Investigator Initiated Study (IIS) ideas/proposals for research grant , ensur ing   that specific   evidence needs are assessed through medical science liais on   and   t he   proposals   are discussed within   local or global   internal committees   collaborating with clinical affairs members .   Regarding   non-clinical studies, c oordinate   and   track the progress on contract,   execution   and publication for studies .       For clinical studies, to   provide   medical   insights on clinical question   and   study design ,   address   the   inquiries   in internal committees , review   manuscripts   and provide   timely   feedback to the study team.   To plan non-clinical studies internally for local evidence generation. Co ordinate   internal committee approval