Data Transparency Lead

UCB; Raleigh (NC); Hybrid; USD 90,000 - 130,000; Full time

Job summary

UCB is seeking a Data Transparency Lead to join the Global Clinical Sciences and Operations team in Raleigh, North Carolina. This hybrid role requires in-office presence of at least 40% of the time.

You will oversee global data transparency activities, ensuring compliance with transparency requirements and alignment with scientific and ethical standards. You will lead the preparation of data and documents for transparency, disclosure, and data sharing, and act as the transparency point of

Responsibilities

• Prepare, lead, and support transparency documents and data anonymization activities.

Job description

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,