Director, Global Trial Master File A global biopharmaceutical company on a mission to Solve On, Incyte follows science to find solutions for patients with unmet medical needs. Through the discovery, development, and commercialization of proprietary therapeutics, Incyte has established a portfolio of first-in-class medicines for patients and a strong pipeline of products in Hematology, Oncology and Inflammation and Autoimmunity.Headquartered in Wilmington, Delaware, Incyte has operations in North America, Europe, and Asia. Job Summary (Primary function) This role provides enterprise leadership for Trial Master File (TMF) strategy, governance, and execution across a global clinical portfolio and is accountable for end-to-end TMF operations, including oversight of internal teams, FSPs, CRO partners, and enabling technologies. The role ensures inspection readiness, regulatory compliance, and scalable operations while driving continuous improvement and modernization of TMF practices. Essential Functions of the Job (Key responsibilities) Strategic Leadership & Governance : Define and lead the global TMF strategy, governance framework, and operating model Establish inspection-readiness standards aligned with ICH-GCP and global regulations Serve as escalation point for TMF risks, compliance issues, and inspection outcomesPeople Leadership : Lead and develop a global team of TMF professionals across regions and partners Drive workforce planning, capability building, and performance management Foster an inclusive culture of accountability, quality, and continuous improvementOperational Oversight : Ensure consistent TMF execution across studies, CROs, and regions Own KPIs, quality metrics, and timeliness of TMF deliverables Oversee TMF consolidation, archival, and retention strategiesInspection & Audit : Lead TMF support for regulatory inspections and internal audits Review findings, approve CAPAs, and ensure sustainable remediationProcess & Innovation : Own global TMF SOPs, work instructions, and TMF Index Model Drive system optimization (e.g., Veeva Vault) and digital innovation Leverage automation and data insights to improve TMF quality and efficiency Qualifications (Minimal acceptable level of education, work experience, and competency) Degree (such as Bachelor's) or equivalent experienced required; advanced degree or equivalent experience preferredSignificant experience in TMF or clinical document management (typically 8-10+ years, or equivalent experience)Experience managing global teams and vendorsStrong knowledge of ICH-GCP and regulatory requirementsExperience with eTMF systems (such as Veeva Vault, or similar systems)Familiarity with CDISC TMF Reference ModelStrong leadership, communication, and problem-solving skillsExperience in global, matrixed organizationsWillingness to travel up to 20%, both domestic and international. Reasonable accommodations will be provided to support candidates with disabilities.Disclaimer: The above statements are intended to describe the general nature and level of work performed by employees assigned to this job. They are not intended to be an exhaustive list of all duties, responsibilities, and qualifications. Management reserves the right to change or modify such duties as required.Incyte Corporation is committed to creating a diverse environment and is proud to be an equal opportunity employer.
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