Data Management Programme Lead

Julius Clinical is a leading global, full-service Clinical Research Organization (CRO) delivering integrated clinical development and real-world evidence solutions across five continents. Formed through the strategic merger of P95 and Julius Clinical, the organization combines P95's leadership in infectious diseases, vaccines, and real-world evidence with Julius Clinical's expertise in central nervous system, cardio-metabolic, renal, and rare diseases, creating a unique mid-sized CRO with scale, agility and scientific depth. With regional hubs in Africa, Latin America, North America, Southeast Asia, and Europe, we operate with a team of 500 professionals and a track record that includes more than 1000 clinical trials conducted in over 50 countries. We offer comprehensive CRO capabilities supporting both full-service and modular approaches across the entire development lifecycle and post-marketing phases for pharmaceutical, biotech, and public health partners.

P95 JC is seeking an experienced and motivated Data Management Programme Lead to take ownership of a dedicated sponsor portfolio, providing leadership across one or more clinical studies while serving as a trusted partner to the sponsor.
This is a hands-on leadership role that combines Clinical Data Management expertise, programme oversight, sponsor engagement, team development, and operational planning. The successful candidate will work closely with both sponsor stakeholders and internal teams to ensure high-quality, efficient, and compliant delivery of Data Management activities throughout the study lifecycle.
The Data Management Programme Lead will play a key role in driving delivery excellence, building strong sponsor relationships, supporting team growth and development, and continuously improving ways of working to ensure successful study outcomes.

• Act as the primary Data Management contact for an assigned sponsor or sponsor programme
• Develop and maintain strong, collaborative relationships with sponsor stakeholders
• Provide strategic and operational oversight across one or more clinical studies
• Lead or contribute to sponsor governance meetings, study planning discussions, and operational reviews
• Proactively identify risks, issues, and opportunities, driving timely resolution and continuous improvement
• Support, mentor, and develop Data Management professionals working on the assigned programme
• Foster a culture of accountability, collaboration, quality, and continuous learning
• Support study budget oversight, forecasting, and resource planning activities
• Monitor programme performance and utilisation to support efficient delivery
• Champion data quality, inspection readiness, and compliance across assigned studies
• Identify opportunities to improve efficiency, processes, and standardisation
• Contribute to departmental initiatives that strengthen Data Management capabilities and service delivery

• Extensive experience (minimum of 6 years) within Clinical Data Management in a CRO, pharmaceutical, biotechnology, or clinical research environment,
• Experience leading Data Management activities across multiple clinical studies or programmes
• Experience working directly with sponsors and building strong client relationships
• Experience coordinating or leading teams, projects, programmes, or functional initiatives
• Expert knowledge of clinical trial processes across start-up, conduct and close-out
• Experience driving process improvements and implementing best practices within Data Management
• People leadership, mentoring, coaching, or team development activities 
• Strong problem-solving and decision-making skills
• Fluency in English, both written and verbal