Descripción de la oferta
Centurion, South AfricaBelgrade, SerbiaLisbon, PortugalBratislava, SlovakiaZagreb, CroatiaBarcelona, SpainSofia, BulgariaMadrid, SpainFull timeSite Activation Manager, Global Study LeadershipAt IQVIA, our Site Activation Managers play a critical role in bringing new therapies to patients faster. As part of the Global Study Leadership team, you'll lead site activation activities across global clinical trials, working with sponsors, sites and cross-functional teams to drive study start-up success. It's an opportunity to make a global impact while advancing your career in clinical research leadership.Why Join Global Study Leadership?Global Study Leadership is a global, full-service team delivering clinical trials through both therapeutically aligned and customer-dedicated delivery units. You'll work across diverse therapeutic areas and partner with leading pharmaceutical and biotechnology companies, gaining exposure to a broad range of studies, countries, regulatory environments and delivery models.With structured career development, tailored training, mentorship and opportunities to grow across Site Activation, Clinical, Project Management, and Oversight roles, you'll build expertise that accelerates your career. Supported by a collaborative culture, flexible working environment and AI-enabled technologies, you'll help drive efficient study delivery while bringing new treatments to patients worldwide.What You'll Be DoingYou'll lead study start-up activities across global, regional, and country-level programs, ensuring studies are activated efficiently, compliantly, and on schedule. Working as part of an integrated cross-functional team, you'll partner with sponsors, sites, and stakeholders worldwide to accelerate patient enrolment and drive successful clinical trial delivery.Key ResponsibilitiesLeading site identification, feasibility, regulatory submissions, ethics approvals and site contractingDeveloping and executing Site Activation Management Plans aligned to study strategy and objectivesPerforming protocol amendmentsDriving study start-up timelines and critical milestonesManaging regulatory strategies, approvals and essential study documentationNegotiating contracts and regulatory documents while ensuring local and global complianceIdentifying risks, resolving issues and implementing mitigation plansBuilding strong relationships with sponsors, sites, and cross-functional stakeholdersMonitoring project metrics, budgets, timelines and performance indicatorsProviding project updates, reports, presentations and operational insightsSupporting proposal development, bid defence activities and customer engagementMentoring colleagues and contributing to continuous improvement initiativesWhat We're Looking ForBachelor's degree in Life Sciences or a related fieldExperience in site activation, study start-up, protocol amendments, regulatory affairs or clinical operationsStrong knowledge of ICH-GCP, clinical trial regulations, ethics processes and regulatory requirementsExperience managing timelines, budgets, risks and cross-functional stakeholdersStrong communication, negotiation and stakeholder management skillsAbility to lead complex projects and drive outcomes in a global environmentStrong planning, organizational and problem-solving skillsExperience working across cultures and geographiesPassion for innovation and leveraging technology to improve clinical trial deliveryBuild Your Future with IQVIAIf you're looking for a role that combines global exposure, strategic influence, meaningful work, and clear career progression, we'd love to hear from you. Join a team that partners with some of the most innovative organizations in healthcare, leverages cutting-edge technology to transform clinical research and is committed to improving patient outcomes worldwide while supporting your long-term career growth.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.ComIQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.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#J-18808-Ljbffr
