Site Management Intern

Site Management Intern Job Description

A great opportunity for students eager to begin a career in Clinical Research and gain handson 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 teamled trainings workshops and knowledgesharing 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 decisionmaking in real study environments.
• Gain exposure to study monitoring riskbased monitoring concepts and site relationship management.
• Assist with preparation for visits followup tasks and tracking activities.

Site Monitoring & Field Exposure

• Opportunity to observe onsite 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 crossfunctional 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

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.