Project Manager - Wansford Commercial Research Delivery Centre (CDRC)
| Dyddiad hysbysebu: | 19 Chwefror 2026 |
|---|---|
| Cyflog: | Heb ei nodi |
| Gwybodaeth ychwanegol am y cyflog: | Negotiable |
| Oriau: | Llawn Amser |
| Dyddiad cau: | 16 Mawrth 2026 |
| Lleoliad: | Wansford, PE8 6PL |
| Cwmni: | NHS Jobs |
| Math o swydd: | Cytundeb |
| Cyfeirnod swydd: | A1881-26-0001 |
Crynodeb
Programme Administration and Coordination Coordinate meetings, workshops, and forums across the CRDC-PC network including the Executive Committee, the Steering Group and the Operational Group Maintain comprehensive programme documentation, tracking progress against key milestones, metrics, and deliverables Assist with grant management activities including budget monitoring and reporting Coordinate and monitor project activities in line with agreed plans and milestones Network Support and Communication Help establish and maintain the Digital Community platform in MS Teams as the cornerstone of network collaboration Coordinate training programmes and capacity building initiatives across Spokes and Delivery Hubs Support the development and distribution of standardised resources, templates, and best practice materials Facilitate knowledge exchange between experienced and developing sites Stakeholder Engagement Provide administrative support for Sponsor Access Forums and bilateral meetings with pharmaceutical partners Assist with Patient and Public Involvement and Engagement (PPIE) activities and Community Advisory Forum coordination Support liaison activities with NIHR, ICB partners, and other stakeholders Help coordinate Research Inclusion workshops and community engagement events Data Management and Reporting Maintain programme databases and tracking systems Assist with the development of monitoring and evaluation frameworks Support the preparation of progress reports for NIHR and other stakeholders Help collect and analyse data for programme impact assessment Quality Assurance and Compliance Support sites with compliance requirements including GDPR, NCVR, and regulatory frameworks Assist with mock site inspections and quality audits Help maintain Investigational Medicinal Product management processes and confidentiality agreements Support the development of Standard Operating Procedures