2026 CRA DP Beijing Shanghai

IQVIA

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profile Job Location:

Beijing - China

profile Monthly Salary: Not Disclosed
Posted on: 3 hours ago
Vacancies: 1 Vacancy

Job Summary

Job Overview
Engage in structured training program to gain knowledge and skills required to independently conduct clinical monitoring visits in accordance with study protocol standard operating procedures good clinical practice and applicable regulatory requirements.

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 () with a bachelors 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

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.

Job OverviewEngage in structured training program to gain knowledge and skills required to independently conduct clinical monitoring visits in accordance with study protocol standard operating procedures good clinical practice and applicable regulatory requirements.Essential FunctionsComplete requir...
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About Company

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IQVIA is the Human Data Science Company™. We are inspired by the industry we serve and provide solutions that enable life sciences companies to innovate with confidence, maximize opportunities and ultimately drive human health outcomes forward. Our approach is Human Data Science – a d ... View more

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