# 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-1-2-Sr_R1554272?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/jobs/job_91a9c505-231

## Description

As a member of the research team at the research centre, you will coordinate and execute assigned clinical trials according to the study protocol, agreed upon scope of work, GCP, sponsor/company SOPs, and relevant guidelines and regulations.

Responsibilities:

- Work as a research team member at the research centre, following regulatory requirements, agreed upon scope of work, applicable SOPs, work authorizations, and study protocols.

- Assist investigators with feasibility questionnaires and case report forms.

- Facilitate site initiation: assist sites with screening visits, submission of documents to ethics committees for approval, and dispensing of investigational products.

- Assist investigators with subject screening and enrolment.

- With investigator authorization, assist with follow-up visits and procedures as required by the protocol, including scheduling, inventory checks, and other coordination tasks.

- Manage investigational products, study materials, and laboratory samples at the research centre.

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

- Assist investigators with archiving study documents and submitting them to ethics committees or other authorities.

- Accurately transcribe data from source documents to case report forms and assist with query resolution.

- Facilitate site closure: assist sites with closure visits, collection of investigational products and study materials, and archiving of study documents.

- Create and maintain routine reports and other work-related documents.

- Travel to other cities may be required as needed.

Requirements:

- Basic knowledge of clinical research and applicable regulatory requirements.

- Familiarity with medical terminology.

- Good communication and organizational skills.

- Proficient in Microsoft Office software.

- Fluent in Chinese, with basic English proficiency.

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

- Strong confidentiality skills.

Education and Experience:

- Associate's degree or higher in clinical medicine, pharmacology, nursing, healthcare, or related field.

- Less than 1 year of experience as a clinical research coordinator.

- Experience working in clinical research or the pharmaceutical industry.

## Skills

### Required
- clinical research
- GCP
- Microsoft Office
- Chinese
- English
- medical terminology

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