Descripción de la oferta
Overview We are seeking a highly motivated and skilled Senior Project Manager to join our growing Real-World Evidence (RWE) team. This is a home-based role within Europe , offering flexibility while providing the opportunity to lead global and regional studies. You will lead the planning, execution, and delivery of real‑world evidence studies, including non‑interventional studies, registries, chart reviews, secondary data analyses, and pragmatic research. This role ensures operational excellence, regulatory compliance, and strong stakeholder engagement across global or regional RWE programs. The PM serves as the primary point of accountability for timelines, budget, quality, and cross‑functional coordination. Responsibilities Oversee planning and execution of medium to large, regional or multi-regional clinical studies, ensuring speed, quality, and cost optimization. Serve as the primary point of contact for clients, fostering strong relationships and customer satisfaction. Lead cross-functional teams, driving collaboration and milestone achievement. Develop and implement integrated study management plans. Monitor project progress, mitigate and manage risks, and resolve issues proactively. Ensure compliance with GEP, GVP and local regulations, and company processes. Manage project financials, including forecasting, scope changes, and revenue acceleration opportunities. Mentor and support team members, promoting continuous improvement and knowledge sharing. Lead bid defense presentations and contribute to study strategy development. Experience Experience - ideal candidate Bachelor’s degree in Life Sciences or related field. 5+ years in project management including, +2 years Real-Word Evidence (RWE) Strong knowledge of clinical study conduct, risk management and regulatory requirements. Therapeutic area expertise for Infectious Disease and/or Vaccines. Previous CRO experience required. Effective leadership, mentorship and management skills with attention to details. Demonstrates excellent analytical, organizational and problem-solving abilities. Proven ability to manage complex projects across geographies and functions. Proven ability to develop and manage timelines, tasks, milestones. Experience - you must also have these skills Experience in vendor management and oversight. Experience managing and tracking study budgets and financials with participation and involvement with invoice and contract review and approvals. Excellent oral and written communication, presentation and interpersonal skills Proficiency in MS Office and project management tools. ICH GCP awareness is a plus. Willingness to travel up to 20% as required. About us P95, an Ampersand portfolio company, is a global provider of clinical and epidemiological services related to vaccines and infectious diseases. Founded in 2011, we are a leader in sourcing, analyzing, and reporting epidemiological data to assist health agencies and pharmaceutical companies in improving access to safe and effective vaccines. Headquartered in Belgium, P95 has also offices in Europe, North America, South America, South Africa, and SE Asia. We are passionate about healthcare and helping our customers with innovative medical research. We share a sense of urgency with our customers to deliver timely, pragmatic and useful insights to improve healthcare. Our clients are from the pharmaceutical industry, public health institutes, academic institutions, WHO, the European Commission and other governmental organizations and Non-Governmental Organizations (NGOs). Our projects focus mainly on infectious diseases, particularly on vaccines. #J-18808-Ljbffr
