Executive Director, Clinical QA

## Who We Are : At Neurocrine Biosciences, we pride ourselves on having a strong, inclusive, and positive culture based on our shared purpose and values. We know what it takes to be great, and we are as passionate about our people as we are about our purpose - to relieve suffering for people with great needs.## What We Do : Neurocrine Biosciences is a leading neuroscience-focused, biopharmaceutical company with a simple purpose : to relieve suffering for people with great needs. We are dedicated to discovering and developing life-changing treatments for patients with under-addressed neurological, neuroendocrine and neuropsychiatric disorders. The company's diverse portfolio includes FDA-approved treatments for tardive dyskinesia, chorea associated with Huntington's disease, classic congenital adrenal hyperplasia, endometriosis\

• and uterine fibroids,\
• as well as a robust pipeline including multiple compounds in mid- to late-phase clinical development across our core therapeutic areas. For three decades, we have applied our unique insight into neuroscience and the interconnections between brain and body systems to treat complex conditions. We relentlessly pursue medicines to ease the burden of debilitating diseases and disorders because you deserve brave science. For more information, visit , and follow the company on , and . (
• in collaboration with AbbVie
• About the Role :
• Provides vision, strategic planning and management for departmental initiatives. Responsible for developing and setting strategy and operating plans for Clinical QA, and establishing compliance, procedures, and quality leadership. Responsible head for the Clinical QA matters for building and leading a team of highly trained and skilled quality professionals in order to implement the quality systems and perform activities necessary to ensure compliance and to ensure QA support of clinical study teams. Prepares and leads the company through pre-approval inspections and clinical audits. Coordinates interdepartmental activities both internally and externally with regulatory, clinical, drug safety, and medical affairs to ensure clinical activities and internal functions meet quality standards and reflect risk-based principals. Ensures budget, schedules, and department performance requirements are met. Additionally, mentors and coaches all employees within the QA group and provide leadership and management within the entire team.\_##
• Your Contributions (include, but are not limited to) :
• Drives the strategic vision and direction for Clinical QA group
• Develops, executives, evaluates and adjusts strategy for Clinical QA and establishes strong, effective working relationships with internal and external stakeholders to achieve GCP compliance and Quality objectives
• Leads effort in developing, implementing and communicating of the GCP QA vision, goals, core capabilities, and values while championing a strong Quality Culture
• Partners with Clinical Development, Clinical Operations, Biostatistics, Pharmacovigilance, and Regulatory Affairs stakeholders regarding compliance issues and provides quality guidance and expert interpretation of GCP regulatory requirements and expectations
• Responsible for preparations and direct participation in regulatory inspections, which may include reviewing inspection readiness planning, mock inspections, performance of pre-approval inspections, and risk-based management of program inspection quality events
• Leads and project manages the development, implementation, and enhancements to the clinical QMS
• Participates in the evaluation, selection, compliance audit strategy, and oversight of global clinical investigators, contract clinical laboratories, and CROs
• Monitors the regulatory status of principal investigators and intervenes when sub-optimal performance is identified. Assists in remediation and corrective action plans to ensure all parts of the study are conducted properly
• Supports investigational new drug applications, ex-US clinical trial applications (CTA), and related correspondence from global regulatory authorities
• Develops metrics and trending of compliance activities for Clinical Quality Assurance and communicate these to upper management as necessary
• Performs investigator site and vendor audits to assess the integrity of the study data and to determine if studies are being conducted in compliance with applicable GCP / regulatory requirements and guidelines, study protocols, monitoring plans and applicable policies / procedures
• Directs and oversees compliance activities related to drug safety and pharmacovigilance, phase IV studies and investigator-initiated trials
• Oversees and may perform the internal audits designed to determine if policies / procedures, systems, reporting and / or the conduct of the investigational studies are executed with compliance to GCP principles / regulations
• Other duties as assigned##
• Requirements :
• RN, BSN, BS / MS, or BA degree or equivalent experience in scientific or health care field and 17+ years of industry experience including GCP leadership roles within a development and commercial GCP environments. Extensive GCP audits and inspections or related experience required. Experience with developing and implementing GCP QA systems, process’ and procedures. Previous managerial experience also required OR
• Masters Degree in similar field as noted above and 15+ years of experience as noted above
• In-depth knowledge of all Clinical Trial related FDA regulations, ICH Guidelines, and experience with international GCP regulations and guidelines is required
• Ability to create a comprehensive audit program and carry out audits of investigator sites and clinical research vendors for Phase I-IV studies. Requires an in-depth knowledge of auditing principles, techniques and communication skills to clearly and efficiently convey findings and report deficiencies to investigator sites as well as management
• Ability to work closely with both internal and external personnel to increase the level of compliance and cooperation while creating opportunities to improve operations and implementation
• Excellent understanding of domestic and international regulations and guidance documents, with a focus on FDA & EMA regulations
• Strong pharmaceutical industry experience with a working knowledge of quality systems and regulatory compliance requirements for clinical quality assurance
• Strong knowledge of all regulations pertaining to GxP’s and current industry trends as related to pharmaceutical, biological and gene therapy products
• Demonstrated knowledge and expertise in GCP, as well as GLP and / or GMP systems throughout the product lifecycle
• Demonstrated analytical ability, strong leadership skills, exceptional communication skills, creativity, and the ability to effectively manage and implement multiple projects
• Ability to solve problems and troubleshoot issues
• Expert at managing complex and multiple work streams in changing circumstances
• Proven ability to cultivate and develop relationships with cross functional teams and vendors
• Demonstrated leadership ability to identify, manage and develop QA teams
• Recognized as an internal thought leader with extensive technical and business expertise within a strategic organization
• Demonstrated in-depth knowledge of own function, business / commercial / scientific expertise to solve critical issues successfully and innovatively
• Evaluates key business / scientific challenges and completes complex, ambiguous initiatives having cross-functional impact
• Excellent interpersonal skills and competent confident communication when interacting with regulatory authorities as well as internal leaders and external partners
• Analyzes complex situations / issues and effectively communicate situations / issues, along with potential recommendations, to various functional groups
• Provides mentorship, acts as a trusted advisor, and is an advocate for Quality

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