We are looking for a Lead Clinical Project Manager to join our Global Clinical Sciences and Operations team, based in our Raleigh, NC office. This is a hybrid role (at least 40% of the time in office). About the role The Lead Project Manager will be accountable for the delivery of patient-centric studies from protocol design through to study report and archiving. These can be all types of study from First in Human to Phase IV, across all geographies and in all UCB therapeutic areas including Gene Therapy. Lead CPMs will be accountable for complex studies across geographies in therapeutic areas/assets that are considered as priority for UCB and/or multiple studies running in parallel. They will also be accountable for the effective interface and influential stakeholder management between UCB, Phase 1 Units, Clinical Research Organizations (CROs) and other vendors to ensure assigned studies are delivered according to contract specifications, with high quality, meeting all major milestones and to budget. Who you'll work with The Lead CPM closely cooperates with the Program Delivery Lead (PDL). In certain scenarios, the Lead CPM may act as the PDL if, for example, there is only one study on a program or for a NIS primary data capture study. In this scenario, the Lead CPM will be additionally accountable for the study concept planning ensuring alignment to the Clinical and Operational Development Plans. What you'll do - Accountable for the leadership and delivery of all assigned UCB sponsored clinical trials through effective internal and external team stakeholder management in a matrix organisation. - Responsible for operational updates, issue/mitgations, ensuring open, transparent communication with team members, line management and Clinical Strategic Partnering, escalating within and outside the team as needed. - Demonstrate robust oversight of sponsor-delegated activities by regularly reviewing CRO/Phase 1 Unit performance, including TMF status, through use of KPIs, metrics and deliverables (such as SQV, Impact), with a focus on trial subject safety, data quality, and critical activities that might delay the project or impact budget. - Responsible for Site Engagement strategies to support study recruitment at sites. Become familiar with the competitive landscapes; engage with Key Opinion Leaders (KOLs), investigational sites, patient advocacy groups and other relevant organizations. - For assigned studies, be the key internal clinical operations contact, working closely with the respective PDL and other team members. - In certain scenarios, the Lead CPM may act as the PDL if, for example, there is only one study on a program or for a NIS primary data capture study. - During start-up, articulate study scope, goals, and expectations of UCB to the CRO/Phase 1 Unit and ensure all relevant information that may impact the set-up of the trial is highlighted and accounted for in the study planning. - Responsible for detailed planning of study timelines to enable timely access and prompt decision making for all data for Safety Monitoring/Data Monitoring Committees, planned Interim Analyses, final data reporting for Results Interpretation Meetings and final Clinical Study Report (CSR). - Responsible to manage, track and ensure accuracy of study budgets in UCB systems, including the forecast and accrual information. - Work with CRO partners to define a study specific monitoring strategy. Review Monitoring Plans, and CRA generated reports (as appropriate). - Support any audit/inspection activities, including audit/inspection readiness, ensuring findings are appropriately addressed in a timely manner and overall compliance with regulations (eg, ICH GCP) and applicable quality standards at all times. - Identify issues/gaps in processes and interfaces with other groups and departments and develop recommendations for resolution. Contribute to process improvement initiatives, and share best practice experiences with line manager, peers and Partner CROs. - Mentor CPM/Senior CPMs in operational aspects of study conduct, as needed Interested? For this role we're looking for the following Minimum requirements - Bachelor's Degree - 10 years' relevant experience in clinical development including team leadership. - Experience or capability to manage in-house and/or outsourced regional or global Phase 3 studies (First in Human to multicentre clinical studies) from study start-up to study report completion Preferred requirements - A Lead CPM must have substantial experience in study management in different indications and proven ability to manage complex multinational studies or multiple simultaneous studies from start to end. - A Lead CPM must have proven record of high impact on study delivery in high visible, high complex challenging global studies. - A Lead CPM is known as an expert in managing studies. They can provide guidance, troubleshoot and answer questions related to their area of expertise. They also demonstrate initiative and adaptability to special problem situations, and challenges. This position reasonably anticipated base salary range is $148,000-195,000K. The actual salary offered will take into account related knowledge, skills, experience and location among other factors and may fall outside the expected range. Are you ready to 'go beyond' to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!