For our _Real World Solutions Team_ based in **Prague** , we are looking for a **Real World Evidence (RWE) Associate Project Manager** . **Open Position Description** IQVIA is seeking a dynamic and experienced **Associate** **Project Manager** to lead and coordinate _Real World Evidence (RWE) projects_ in the Czech Republic and CEE region. This role is ideal for a professional with vertical expertise in RWE, including _observational studies_ , _patient registries_ , and _clinical protocol development_ , who can manage cross-functional teams and ensure successful project delivery. **Responsibilities:** + Coordinate, organize and plan observational study activities, managing timelines and projects’ quality while ensuring projects are delivered on budget + Manage consistency of data sources with direct interactions with all the actors involved in the studies + Coordinate junior IQVIA resources and external stakeholders (from the clinical side) + Oversee (from a PM perspective) all activities related to CRF systems, protocol definition, patient registries, relations with clinical sites, etc. + Manage clients’ communication + Help organizing the work of junior team members and ensuring quality controls on projects + Collaborate with internal and external stakeholders to define project scope, timelines, and deliverables. + Ensure compliance with clinical protocols, regulatory requirements, and IQVIA’s quality standards. + Manage project budgets, timelines, and resources, ensuring optimal allocation and performance. + Serve as the primary point of contact for clients, providing regular updates and strategic guidance. + Coordinate with data management, biostatistics, medical writing, and regulatory teams to ensure seamless project execution. + Identify risks and implement mitigation strategies to ensure project success. **Requirements** + Bachelor’s or Master’s degree in Life Sciences, Public Health, Pharmacy, or a related field with deep expertise on clinical research world + 3+ years working experience in project management within the healthcare or life sciences industry, preferably in RWE or observational research (CROs, regulatory, Pharmacovigilance) + Ability to coordinate projects and resources + Good expertise on clinical data management + Excellent Microsoft Office Skills: strong skills in working with Excel and Power Point + Proficiency in English and Czech, both oral and written + Strong communication skills, both oral and written + Ability to manage multiple projects, juggle priorities and deliver on tight deadlines + Affinity for a collaborative, team-oriented environment + Critical thinking and problem-solving attitude Location: Prague – Hybrid contract IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide. To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us. EEO Minorities/Females/Protected Veterans/Disabled