# Data Transparency Lead at UCB

UCB is hiring a Data Transparency Lead in Raleigh, United States. It pays $148k a year and Level rates it Little AI ●○○○; you can [apply on UCB](https://jobsbylevel.com/go/60f0162f-4ead-430b-809e-9fb086724759?utm_medium=ai-agent).

AI Level 1, AI centrality 38 out of 100. Raleigh, North Carolina, United States.

## Details

- Company: [UCB](https://jobsbylevel.com/companies/ucb)
- AI level: AI Level 1 (score 38 out of 100)
- Location: Raleigh, North Carolina, United States
- Salary: $148k
- Posted: October 23, 2026
- Apply: https://jobsbylevel.com/go/60f0162f-4ead-430b-809e-9fb086724759?utm_medium=ai-agent
- Free CV review for this job: https://jobsbylevel.com/cv-review?job=data-transparency-lead-at-ucb-62924b

## Description

Make your mark for patients We are looking for a Data Transparency Lead to join our Global Clinical Sciences and Operations team, based in our Raleigh, North Carolina office. This is a hybrid role (at least 40% of the time in office). About the role As the Data Transparency Lead, you will oversee global data transparency activities, ensuring compliance with transparency requirements and alignment with scientific and ethical standards. You will lead and support the preparation of data and documents for transparency, disclosure, and data sharing. The Data Transparency Lead will represent the organization as the transparency point of contact, both internally and externally, to provide input and guidance on related activities that represent industry best practices, including input on data elements that are useful and can be shared with statistical perspective (e.g., anonymization, data sharing, disclosure, etc.) Who you’ll work with Develop and maintain efficient working relationships with contributing stakeholders (eg, Clinical Project Management, Biostatistics, Medical Writing, Regulatory Affairs,Safety, Information Technology). Interact frequently with the clinical development teams (Clinical Project Managers, Clinical Program Directors, and Biostatisticians) to ensure awareness of transparency requirements and the need for integration of planning to enable updated clinical trial protocol and results information availability within the mandated timeframes to meet transparency requirements. Support the Disclosure, Quality Control, Medical Writing Teams as needed. What you’ll do Prepare, lead, and support transparency documents and data anonymization activities, including plain language summaries, data sharing, redactions, anonymization, and regulatory submissions in compliance with Standard Operating Procedures (SOPs), FDA EMEA, ICH, and other relevant regulations. Collaborate closely with team members and UCB stakeholders to ensure data sharing activities comply with UCB policies and regulatory requirements. Ensure anonymized submissions and study documentation meet regulatory standards. Oversee external vendors to ensure high-quality, timely deliverables. Manage documents and interface with UCB systems to maintain final documents, track activities, and meet deadlines. Maintain Commercially Confidential Information (CCI) master lists and redaction checklist and provide quality control (QC) of vendor activities to ensure quality and consistency. SME for patient-level data anonymization and privacy-related issues and identify process improvements and solutions with the ability to explain complex and technical topics to key internal stakeholders. Contributes to and manages data anonymization and data sharing timelines and commitments to timelines for the study and/or project. Provide support and input into the development of SOPs, processes, and training to support Data Transparency. Oversee project teams to ensure adherence to UCB’s established Data Transparency Policy and SOPs. Monitor the external landscape and regulatory environment to identify and support updates that may be needed to UCB’s Data Transparency policy. Interested? For this role we’re looking for the following Minimum requirements 5+ (with Master’s degree) or 7+ (with Bachelor’s degree) years area of discipline (data disclosure and transparency roles) within Pharma or Biotechnology (including clinical research organizations) with specialized knowledge in patient-level data anonymization. Preferred requirements Advanced experience in clinical studies design and analysis, including drug development phases, efficacy and safety assessments. In-depth knowledge of global disclosure, transparency, and data sharing. Excellent written and verbal communication skills and ability to communicate complex quantitative ideas clearly. Extensive experience in communicating with all levels of personnel across various departments in domestic and international environments. Ability

The description is cut here. Read the full offer: https://jobsbylevel.com/jobs/data-transparency-lead-at-ucb-62924b

Source: https://jobsbylevel.com/jobs/data-transparency-lead-at-ucb-62924b

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