Sumitomopharma · RemotePrepare for this interview
EliteAI-generated questions, company research, and talking points tailored to this role
Sumitomo Pharma Co., Ltd. is a global pharmaceutical company based in Japan with key operations in the U.S. (Sumitomo Pharma America, Inc.), Canada (Sumitomo Pharma Canada, Inc.) and Europe (Sumitomo Pharma Switzerland GmbH) focused on addressing patient needs in oncology, urology, women's health, rare diseases, psychiatry & neurology, and cell & gene therapies. With several marketed products in the U.S., Canada, and Europe, and a diverse pipeline of early- to late-stage assets, we aim to accelerate discovery, research, and development to bring novel therapies to patients sooner. For more information on SMPA, visit our website https://www.us.sumitomo-pharma.com or follow us on LinkedIn . Job Overview We are currently seeking a dynamic, highly motivated, and experienced individual for the position of Senior Medical Director, Clinical Research (Ophthalmology) to join our R&D Organization. This individual will contribute to the design and execution of clinical development plan(s) for assigned asset(s) and serve as the Clinical Research Lead for stem cell program within the Ophthalmology therapeutic area. Job Duties and Responsibilities Responsible for and lead all activities related to clinical study design from clinical study concept to clinical study protocol for both early- and late-stage programs Leads or joins multi-disciplinary, multi-regional, matrix team through highly complex decisions Leads and drives strategy for clinical studies for assigned asset(s) within the Ophthalmology therapeutic area Provides oversight of clinical trial conduct, interacting with CROs, medical monitors, and vendors as required, and working with the safety group to ensure adequacy of safety monitoring and reporting Provide clinical input for and participate in study set up and design including data collection tools, data analysis, eCRF design, edit checks, vendor database design plans, etc. Study-level, site-level and subject-level data review and interpretation, including documentation and summarization of findings Serve as the internal medical monitoring for clinical trials Review and provide input for the design of the statistical analysis plans, TLFs, and the clinical data output Contributes to interpretation of clinical trial results and the writing of clinical study reports Contributes to the preparation of Investigator Brochures, annual reports, data collection systems and final reports in compliance with appropriate scientific/regulatory/medical standards Contributes to developing clinical components of BLA/NDAs, sNDAs, MAAs and other regulatory filing documents Contributes to company responses to health authorities and ethics committees for ongoing clinical programs to ensure timely registration and initiation of trials globally Contributes to the development of presentation materials for investigator meetings, health authority meetings, scientific advisory board meetings, and national and international scientific meetings Serve as the subject matter expert for ophthalmology, representing Clinical Research to both internal and external customers 20% domestic and international travel Key Core Competencies Knowledge and understanding of FDA, GCP, and ICH regulations and guidance Thorough and up-to-date knowledge of therapeutic area including trends, advances, understanding of currently available therapies and competitive clinical landscape Experience in conducting global clinical trials in both early- and late-stage clinical development, especially protocol development and trial initiation Experience in regulatory submissions in US; preferred experience in Europe and Japan Demonstrated ability to set clear priorities, lead, influence and build consensus in a multi-disciplined team environment Strong team leadership skills and ability to motivate large multi-functional teams Ability to effectively synthesize, interpret and present scientific information to both internal stakeholders and external medical community High degree of organizational awareness, ability to connect the dots to understand all the interdependencies and big picture Excellent interpersonal and communication skills with the ability to balance multiple tasks and work within a multi-disciplinary team Education and Experience MD (or international equivalent) Board certified or board eligible in ophthalmology Fellowship training in vitreoretinal surgery (preferred) or retina A minimum of 5 years' experience in the pharmaceutical industry, with experience as Clinical Research Lead in Ophthalmology therapeutic area Experience in regenerative cell medicine or gene therapy preferred Prior experience working with Japan organizations is preferred The base salary range for this role is $284,320 to $355,400. Base salary is part of our total rewards package which also includes the opportunity for merit-based salary increases, short incentive plan participation, eligibility for our 401(k) plan, medical, dental, vision, life and disability insurances and leaves
How well this role fits your profile.
Worked at sumitomopharma? Share your experience