从这里开始。
Essential Functions
Complete required therapeutic, protocol, and clinical research training.
Gain experience in study procedures with support from senior clinical staff.
Conduct site monitoring visits (selection, initiation, monitoring, close-out) per scope and GCP.
Train sites on protocol requirements and maintain ongoing communication.
Assess site compliance and escalate quality issues as needed.
Track study progress: regulatory submissions, enrollment, CRFs, and data queries.
Maintain TMF/ISF documentation per GCP/ICH and local regulations.
Support study start-up activities.
Prepare visit reports, follow-up letters, and site management documentation.
Collaborate with study team members on project execution.
Learn and support site-level recruitment planning and progress tracking.
Qualifications
Fresh graduates (2025–2026) with a bachelor’s degree in a scientific or healthcare discipline.
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.
