# Clinical Research Coordinator

**Company**: IQVIA
**Experience**: entry
**Job type**: full-time
**Category**: Research
**Industry**: Healthcare

**Apply**: https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Beijing-China/CRC-Intern-_R1554392?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/jobs/job_287a4dd0-40e

## Description

We are seeking a Clinical Research Coordinator to join our team.

As a Clinical Research Coordinator, you will work as a research team member, following regulatory requirements, agreed-upon scope of work, applicable Standard Operating Procedures (SOPs), work authorization, and study protocols at the research site.

Key responsibilities include:

- Assisting researchers with feasibility questionnaires and retrieving completed questionnaires

- Facilitating study site initiation, including screening visits, submitting documents to ethics committees for approval, and dispensing investigational products

- Supporting researcher with subject screening and enrollment

- After obtaining researcher authorization, assisting with follow-up visits and procedures as required by the protocol, such as planning, verifying medication inventory, and coordinating activities

- Managing investigational products, study materials, and laboratory samples at the research site

- Participating in investigator meetings, monitoring visits, audits, and other meetings within the agreed scope of work

- Assisting researchers with archiving study documents and submitting them to ethics committees or other regulatory authorities

- Accurately transferring data from source documents to case report forms and assisting with query resolution

- Coordinating study site closure activities, including closing visits, retrieving investigational products and study materials, and archiving study documents

- Creating and maintaining routine work reports and other work-related documents

- Providing training and support to researchers and other clinical trial personnel, such as nurses and laboratory technicians

Requirements:

- Knowledge of clinical development and regulatory requirements

- Familiarity with medical terminology

- Strong interpersonal and organizational skills

- Proficiency in Microsoft Office software

- Fluent Chinese speaking and writing skills, with basic English proficiency

- Ability to work independently, prioritize tasks, and solve problems

- Strong confidentiality and integrity

- Bachelor's degree in Clinical Medicine, Pharmacology, Nursing, Healthcare, or related fields

- University English proficiency certificate (Band 4 or above)

IQVIA is committed to integrity in our hiring process and maintains a zero-tolerance policy for candidate fraud.

## Skills

### Required
- clinical research
- regulatory requirements
- medical terminology
- Microsoft Office
- Chinese
- English language

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Source: [Apply at iqvia.wd1.myworkdayjobs.com](https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Beijing-China/CRC-Intern-_R1554392?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply)