Director, Data

Remote Full time Within Otsuka Pharmaceutical Co. exists Otsuka Pharmaceutical Development & Commercialization, Inc. (subsidiary exists the Global Clinical Development (GCD) department. OPDC-GCD are a group of physicians and scientists who lead clinical development activities for Otsuka’s global health-care products. Our responsibilities range from due-diligence evaluations, where we stress-test others’ development plans, to development and implementation of our own global development & commercialization plans (GDCP). The GDCP translates basic research and preclinical pharmacology & toxicology into a streamlined plan for first in man, proof of mechanism, registrational and post-approval trials. Its goal is to efficiently evaluate the product’s potential and probability of success, support an effective commercial launch and plan for meaningful innovations to improve or expand the value of the initial product for our global customers (patients, prescribers and payors). Otsuka is seeking a Director, Global Clinical Development who will be responsible for the design and oversight of clinical research programs and protocols for OPDC products under good clinical practices (GCP). The incumbent will be responsible for the evaluation and clinical development of CNS and Digital Medicine products at different stages of development for a global health-care market. The specific duties assigned to the r Director, Global Clinical Development include the following: Consults with patients or their representatives, clinical, regulatory and scientific leaders and thoughtfully applies their recommendations toward optimizing trial objectives, designs and protocols. Develops focused expertise to serve as an internal medical/scientific consultant to health economic, medical affairs, marketing, regulatory, statistical and other research project team members, and to external regulatory agencies. GDCP) and oversees trials essential for determining the clinical safety, efficacy, medical usefulness and value of drug or medical device product candidates. Acts as the signatory on NDA submissions and clinical study and safety documents. Involved in product life cycle management from the earliest stages of development, constantly seeking innovations to add value strategically. Will help lead and support regulatory filing activities and documents. Providing strategic direction and editing to provide concise, clear and convincing argumentation in all such written and verbal communications. In exceptional circumstances, highly qualified candidates with other clinical/scientific doctorates (e.g. Experience in the pharmaceutical industry or in academic translational clinical research (as a general guideline, 1-3 years for Associate Director level; 3-6 years for Director and 6-9 years for Senior Director levels is typically required depending on type of experience at application). A thorough knowledge of clinical medicine and science management. This entails defining critical objectives clearly and maintaining focus toward achieving business outcomes on time, on budget and with superior quality. This includes facility with the Microsoft suite of programs (Word, Excel, PowerPoint, and Outlook). An advanced understanding of drug development principles and clinical trial implementation, management and reporting is essential and will be further developed, including: Flexibility in working across different therapeutic areas and experience in different stages of clinical development. Working knowledge of associated disciplines, including biostatistics, clinical pharmacology, formulation science, data management, and medical writing. Complete understanding of the global regulatory requirements. Demonstrated experience in successful regulatory filings, while not essential, is an advantage. Working knowledge of the principles of health value creation, including financial assessment (e.g., net present value), project planning and budgeting, market research and commercialization strategies. Dedication to assigned, developed projects and project goals. Willingness to travel 30% of time, over weekends and ability to travel internationally. Stay focused on key strategic objectives, be accountable for high standards of performance, and take an active role in leading change. Make decisions considering the long-term impact to customers, patients, employees, and the business. Patient & Customer Centricity
- Maintain an ongoing focus on the needs of our customers and/or key stakeholders. Seek and value others’ perspectives and strive for diverse partnerships to enhance work toward common goals. Empowered Development
- Play an active role in professional development as a business imperative. This information is provided to applicants in accordance with states and local laws. Application Deadline : Comprehensive medical, dental, vision, prescription drug coverage, company provided basic l