Senior Director, Global Clinical Development Nephrology

Senior Director, Global Clinical Development (GCD)Otsuka is seeking an experienced and visionary Senior Director, Global Clinical Development (GCD), with experience in immunology, who will serve as a clinical leader responsible for the design, execution, and oversight of global clinical development programs. The successful candidate will play a key role in shaping the clinical strategy, leading cross-functional study teams, and ensuring the highest standards of scientific and medical integrity. The incumbent will be responsible for the design and oversight of clinical research programs and protocols for OPDC products under good clinical practices (GCP). The Senior Director, GCD works in a multidisciplinary matrix environment and supports the further development and commercialization of pharmaceutical products, for global launches. This position requires deep understanding of all aspects of the drug development process from early clinical stages to post commercialization, with emphasis on the large global clinical trials and regulatory filing activities. The Senior Director, GCD is responsible for all the clinical development activities for the projects assigned and for the successful implementation and completion of trials leading to NDA, BLA, and/or Global filings.Key Job Responsibilities:Lead the clinical development strategy and execution for assigned programs after proof of concept through late-stage trials and regulatory submissions.Provide medical and scientific leadership to cross-functional study teams and ensure high-quality clinical trial design, conduct, and data interpretation.Serve as the medical lead and subject matter expert for assigned indications.Partner with cross-functional team to ensure trials are conducted in compliance with GCP, regulatory requirements, and internal processes.Lead and contribute to development of clinical sections of regulatory documents, including INDs, IBs, clinical study reports, and NDAs/BLAs.Collaborate with regulatory affairs on interactions with global health authorities.Provides strategic and medical oversight to vendor and CRO relationships and provides clinical input into their governance committees.Lead clinical discussions with KOLs and advisory boards.Develop clinical documents including medical monitoring plans, asset development plansContribute to development of publication plans and review scientific manuscripts for publications.Mentor and provide leadership to junior team members within the organization.Support business development activities through medical due diligence and evaluation of external opportunities.Contributes to corporate initiatives by participating in continuous process improvement to meet companyKnowledge, Skills, Competencies, Education, and Experience:A clinician (M.D., or D.O.) preferably with an immunology, rheumatology, or dermatology background including management experience (direct or indirect). Supplementary degrees (e.g., Ph.D., M.P.H., M.B.A.) are a plus. In exceptional circumstances, highly qualified candidates with other clinical/scientific doctorates (e.g. D.M.D., D.D.S., Pharm.D., Psy.D., D.V.M., or Ph.D. may be considered if complemented by a team or consulting clinician.Experience in the pharmaceutical industry, clinical practice experience and/o academic translational clinical research experience (as a general guideline minimum of five years of clinical research experience, post academia).Requires thorough knowledge of clinical medicine and/or clinical pharmacology and associated disciplines (e.g. biostatistics, data management, medical writing).An advanced understanding of clinical medicine and science.Advanced understanding of drug development principles and clinical trial implementation and management.Complete understanding of the global regulatory requirements.Working knowledge of marketing and commercialization.Complete understanding of overall corporate goals with a fundamental grasp of basic principles to work in a business setting.Demonstrated experience in all developmental phases including evaluation of pre-clinical or in-licensing candidates' potential for meeting an unmet medical need, establishing early clinical safety and proof of concept, conduct of global trials for registration, and implementation of late-stage life-cycle management strategies.Demonstrated experience in successfully leading clinical aspects of regulatory interactions; experience with a successful regulatory filing is a plus.Ability to work across different therapeutic areas and different stages of clinical development.Demonstrated ability to manage and motivate clinical team members (e.g., internal staff and external investigators/consultants).Strong communication and presentation skills.Strong computer skills with demonstrated experience in working with the Microsoft suite of programs (Word, Excel, PowerPoint, and Outlook).Knows how/when to apply organizational policy or procedures to a variety of situations.An advanced understanding of drug development principles and clinical trial implementation, management and reporting are 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 immunology, 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.Physical Demands and Work Environment:Travel (~30-35%)See document Physical Demands and Work Environment for further requirements.Competencies:Accountability for Results - Stay focused on key strategic objectives, be accountable for high standards of performance, and take an active role in leading change.Strategic Thinking & Problem Solving - 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.Impactful Communication - Communicate with logic, clarity, and respect. Influence at all levels to achieve the best results for Otsuka.Respectful Collaboration - 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.Salary Range: $245,454.00 - $381,110.00, plus incentive opportunity.Application Deadline: This will be posted for a minimum of 5 business days.Company benefits: Comprehensive medical, dental, vision, prescription drug coverage, company provided basic life, accidental death & dismemberment, short-term and long-term disability insurance, tuition reimbursement, student loan assistance, a generous 401(k) match, flexible time off, paid holidays, and paid leave programs as well as other company provided benefits.Otsuka is an equal opportunity employer. All qualified applicants are encouraged to apply and will be given consideration for employment without regard to race, color, sex, gender identity or gender expression, sexual orientation, age, disability, religion, national origin, veteran status, marital status, or any other legally protected characteristic. If you are a qualified individual with a disability or a disabled veteran, you may request a reasonable accommodation, if you are unable or limited in your ability to apply to this job opening as a result of your disability. You can request reasonable accommodations by contacting Accommodation Request (EEAccommodations@otsuka-us.com) .Statement Regarding Job Recruiting Fraud Scams: At Otsuka we take security and protection of your personal information very seriously. Please be aware individuals may approach you and falsely present themselves as our employees or representatives. 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