Global Study Start Up Lead

Job Location Parexel Uxbridge, England, United Kingdom 2 days ago Be among the first 25 applicants Job Overview Parexel is beginning to search for an experienced global Start Up Lead/Manager to join one of our key sponsors in the EMEA. In this role you are accountable and responsible for defining, developing and delivering the global study start-up project strategy by partnering with roles across the wider study teams as required. The SSU Lead will be assigned to one or more interventional studies in one or more therapy areas such as oncology, vaccines, internal medicine, rare disease or inflammation and immunology. You will take full responsibility for studies covering at least three regions. Responsibilities Partner with country / site feasibility specialists to incorporate up-to-date intelligence for the planned countries and sites into the overall start-up strategy and site activation plan, most typically on studies with a medium to large country and site footprint. Provide project management of activities directly required to complete all site activations for an assigned study as part of a study management led team to complete all start-up activities for a study. Lead start-up meetings that facilitate alignment of site selection to activation activities performed by country level start-up roles with the endorsed trial optimization plan. Responsible for creating and overseeing the initial baseline and subsequent snapshots of timeline planning within the system which build the overall targets for site activation over time in alignment with the priority of the study in the overall portfolio and overall expectation to deliver to plan with a high degree of probability. In conjunction with study management roles is responsible for ensuring consistent participant compensation for sites and institutions taking part in multiple studies concurrently to eliminate knock-on impact across studies. Act as a key point of escalations for site activation related issues raised by country level start-up roles, seeking to firstly resolve issues directly or triage appropriately to other SUPMs on the study or the study management team, will always follow through to resolution. Identify improvements and efficiencies to site activation processes and share lessons learned broadly with key stakeholders. About Parexel Parexel supports clinical studies across the full range of therapeutic areas, and we have longstanding partnerships with a vast client base. We supported the trials of most of today’s top 50 best-selling drugs, but equally we enable more niche drug developments that are critical to the well-being of many patients. You’ll be an influential member of the wider team. Qualifications Bachelor’s degree and minimum 8 years of relevant global trial SSU experience. Global start-up experience (Exposure across a minimum of North America, Asia and Europe) across multiple therapeutic areas. Concurrent management of complex processes within and across countries in multiple regions of the world. Technical expertise in the use of software for the management of clinical studies (enterprise project management, off the shelf and custom built) including reporting systems (dashboards with associated medium to complex data analysis). Expert ability to comprehend status and adapt communications across a diverse audience. Perform critical path analysis across multiple related project plans, will use key performance indicators to assist in driving overall delivery to operational plan across roles. Will use generative artificial intelligence techniques in daily work. Uses risk management techniques as standard to identify and mitigate key project delivery risks. Critical thinker with strategic planning, analytical and problem-solving skills that responds positively to rapid change. Seniority level Mid-Senior level Employment type Full-time Job function Education and Training Industries: Pharmaceutical Manufacturing, Biotechnology Research, and Hospitals and Health Care #J-18808-Ljbffr