# Site Activation Specialist

Hiring organization: [IQVIA](https://career.thegoodapps.co/organizations/iqvia)

Canonical page: https://career.thegoodapps.co/jobs/6fc0d713-9303-4642-b10b-d1e3f1106d75

Listed on IQVIA's own careers site. Applications go to them directly.

- Seniority: Entry

## Summary

This role coordinates the setup and regulatory preparation for clinical research sites, acting as the main liaison between sites, project managers, and sponsors. It suits someone with clinical research experience who is organized, detail-oriented, and comfortable managing documentation and timelines across multiple studies.

_Our summary, not IQVIA's wording._

## Skills named

Microsoft Office

## Required

- Bachelor's degree in a related field
- 1 year of clinical research experience or equivalent education and training
- Knowledge of clinical systems, procedures, and corporate standards
- Knowledge of medical terminology and regulations
- Knowledge of clinical research processes
- Strong Microsoft Office and email skills
- Effective communication and interpersonal skills
- Ability to work independently and prioritize multiple tasks
- Attention to detail

Apply on IQVIA's site: https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Shanghai-China/Site-Activation-Specialist_R1552468