📍 Beijing, ChinaFull time

About this role

• Under general supervision, serve as Single Point of Contact (SPOC) in assigned studies for investigative sites, Site Activation Manager (SAM), Project Management team, and other departments as necessary. Ensure adherence to standard operating procedures (SOPs), Work Instructions (WIs), quality of designated deliverables and project timelines.
• Perform feasibility, site ID, start up and site activation activities according to applicable regulations, SOPs and work instructions. Distribute completed documents to sites and internal project team members.
• Prepare site documents, reviewing for completeness and accuracy.
• Ensure accurate completion and maintenance of internal systems, databases and tracking tools with project specific information.
• Review and provide feedback to management on site performance metrics.
• Review, establish and agree on project planning and project timelines. Ensure monitoring measures are in place and implement contingency plan as needed.
• Inform team members of completion of feasibility, site ID, regulatory for individual sites.
• Review, track and follow up the progress, the approval and execution of documents, questionnaires, CDA/SIF,  regulatory, ethics, Informed Consent Form (ICF), and Investigator Pack (IP) release documents, in line with project timelines.
• Provide local expertise to SAMs and project team during initial and on-going project timeline planning.
• Perform quality control of documents provided by sites.
• May have direct contact with sponsors on specific initiatives.

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.

Frequently Asked Questions

Is the salary disclosed for the SSU CRA position at iqvia?
The salary for this SSU CRA role at iqvia is not publicly listed. Click "Apply Now" to learn more about the compensation package on their official careers page.
Where is the SSU CRA position at iqvia located?
This SSU CRA role at iqvia is based in Beijing, China. The position is listed as on-site or hybrid. Check the full job description or apply directly to confirm the work arrangement.
Is the SSU CRA role at iqvia full-time or part-time?
This is listed as a Full time position. It is posted as a SSU CRA role at iqvia.
How do I apply for the SSU CRA position at iqvia?
Click the "Apply Now" button on this page. You will be redirected to iqvia's official application portal hosted on workday where you can submit your application directly.
When was the SSU CRA job at iqvia posted?
This SSU CRA position at iqvia was posted on Sep 15, 2026. Apply as soon as possible — early applications are often reviewed first.

You'll be redirected to iqvia's official application page on Workday.