**Site Management Intern – Job Description** **A great opportunity for students eager to begin a career in Clinical Research and gain hands‑on exposure to the work of Clinical Research Associates (CRAs) and Clinical Trial Assistants (CTAs).** **Key Responsibilities** **Training & Onboarding** + Participate in a structured onboarding program covering **Clinical Research** , **ICH-GCP** , **clinical monitoring principles** , and **study operations** . + Complete assigned learning modules and attend team‑led trainings, workshops, and knowledge‑sharing sessions. + Build a foundational understanding of trial phases, safety reporting, regulatory requirements, and quality expectations. **CRA & CTA Role Shadowing** + Shadow experienced CRAs and CTAs to observe daily responsibilities and decision‑making in real study environments. + Gain exposure to **study** **monitoring** , **risk‑based monitoring concepts** , and site relationship management. + Assist with preparation for visits, follow‑up tasks, and tracking activities. **Site Monitoring & Field Exposure** + Opportunity to observe on‑site visits of all major types, including: + **Site Selection Visits (SSVs)** + **Site Initiation Visits (SIVs)** + **Interim Monitoring Visits (IMVs)** + **Close-Out Visits (COVs)** + Observe **IP accountability** , subject reimbursement procedures, source documentation review, and essential document checks alongside CRAs. + Support reconciliation of monitoring findings and action items under supervision. **Documentation & Study Management** + Assist with **eTMF filing** , **document QC checks** , and maintenance of trial trackers. + Help prepare study materials, site communications, and newsletters. + Support regulatory document collection, site staff list updates, and study file organization. + Learn how to work with clinical systems such as CTMS, eTMF, and study portals. **Team Collaboration** + Participate in **Site Management team initiatives** , continuous improvement activities, and internal projects. + Attend team meetings, study calls, and cross‑functional discussions to gain broad exposure to clinical trial operations. + Contribute fresh ideas and support process optimization activities. 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 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