**IQVIA is the Human Data Science Company, committed to advancing human health outcomes.** Join our global team and contribute to the success of clinical trials by ensuring timely and compliant site activation processes. As a **Senior Site Activation Specialist** , you will play a key role in supporting study start-up activities at the country level, working closely with investigative sites, internal teams, and sponsors. **Job Overview** In this role, you will perform tasks related to **Site Activation (SA)** and **maintenance activities** in accordance with local and international regulations, SOPs, project requirements, and budgetary guidelines. You’ll work under moderate supervision, contributing to process improvements and supporting project delivery across multiple studies. **Key** **Responsibilities** + Act as the **Single Point of Contact (SPOC)** for assigned studies, liaising with investigative sites, Site Activation Managers (SAMs), Project Managers, and other stakeholders + Conduct **feasibility, site identification, start-up, and activation activities** in compliance with applicable regulations and SOPs + Prepare and review site documents for completeness and accuracy + Distribute finalized documents to sites and internal project teams + Maintain internal systems, databases, and tracking tools with accurate project-specific information + Monitor and report on **site performance metrics** , providing feedback to management + Collaborate on project planning and timelines, implementing contingency plans when needed + Track and follow up on the progress, approval, and execution of key documents including CDAs, SIFs, regulatory submissions, ethics approvals, ICFs, and IP release documents + Provide **local regulatory expertise** to SAMs and project teams during planning and execution phases + Perform **quality control** of site-submitted documents + May engage directly with sponsors on specific initiatives **Qualifications** + Bachelor’s degree in Life Sciences or a related field + Minimum **3 years of clinical research or relevant experience** , including at least **1 year in a leadership capacity** + Strong understanding of clinical trial processes and regulatory requirements + Excellent organizational, communication, and problem-solving skills + Proficiency in MS Office and clinical trial management systems + Ability to work independently and collaboratively in a fast-paced environment + Fluent in English (additional languages are a plus) **What We Offer** + Career development opportunities and access to world-class training + Supportive leadership and flexible work arrangements + Exposure to a wide range of therapeutic areas and global projects + A stable and reputable international company culture + Competitive benefits package 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