Director, Clinical Operational Data Governance

Role Overview: The Director, Clinical Operational Data Governance at GSK plays a crucial role in driving the governance and management of clinical operational data to support groundbreaking research and development efforts aimed at delivering transformative medicines. Your primary responsibility will be to ensure the availability of high-quality operational data from clinical studies, supporting informed decision-making for current and future clinical pipeline activities. As a key player in shaping the future of healthcare, you will play a pivotal role in ensuring the integrity and accessibility of operational data that drives our clinical studies, ultimately enabling us to bring innovative treatments to patients more efficiently. Key Responsibilities: - Serve as the Global Process Owner/Lead for processes related to clinical operational data intake, management, and downstream provisioning. - Act as the Clinical Technology Lead to ensure the maintenance of an optimal technology landscape that supports the execution of business processes related to clinical operational data. - Lead data governance activities as the Domain Owner for the study-level Clinical Operational Data Domain. - Collaborate closely with stakeholders to maintain data integrity, reliability, and compliance with regulations and standards. - Oversee the collection, storage, and maintenance of clinical operational data, ensuring it is organized and accessible for analysis and reporting. - Manage stakeholder relationships, communication, and continuous improvement efforts to foster a culture of accountability, collaboration, and data quality awareness. - Lead cross-functional projects and identify opportunities to enhance data management processes through advanced analytics and automation. Qualifications Required: - Bachelor's degree in Information Systems, Life Sciences, Data Science, or a related field. - At least 10 years of experience in the pharmaceutical or life sciences industry in data management and governance. - Strong industry experience in clinical trial processes, regulatory requirements, and data governance principles. - Proven track record in stakeholder management and leading cross-functional teams. (No additional details of the company were present in the job description.),