# Clinical Research Coordinator

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

**Apply**: https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Taipei--Taipei-City-Taiwan/XMLNAME-18287-Assoc-Patient---Site-Svcs-Mgr_R1232926?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/jobs/job_9bb84968-39b

## Description

We are seeking a Clinical Research Coordinator to perform, manage, and coordinate activities for assigned opportunities and projects.

You will be responsible for:

- Conducting data mining and analysis to formulate recommendations for internal and external stakeholders

- Training and supporting new team members and junior staff

- Making recommendations for process improvements

Key responsibilities include:

- Ensuring IQVIA planning services provide a competitive edge in winning new business

- Developing accurate and robust country, site, or enrollment strategies for opportunities, including requests for proposals and awarded studies

- Supporting the development of materials for feasibility or site lists, or enrollment strategies for customer bid defense meetings

- Collaborating with key stakeholders and IQVIA project teams to resolve issues

- Preparing for planning meetings by conducting research into therapeutic areas using databases, scientific literature, and expert medical knowledge

- Leading planning meetings with internal stakeholders, including Medical Directors, Therapeutic Strategy Leads, Business Developers, Sales Staff, and Program Directors

- Undertaking therapeutic training as necessary and staying up-to-date with developments in clinical research

- Training and supporting new team members

Requirements:

- Bachelor's degree in Healthcare or Biological Science

- 3 years of related experience in clinical research, or an equivalent combination of education, training, and experience

- Clinical/project management experience is preferred

- General knowledge and understanding of company clinical systems, procedures, and corporate standards

- Good knowledge of medical terminology, GCP, FDA regulations, and the Drug Development process

- In-depth understanding of clinical research

- Excellent communication, organizational, and interpersonal skills

- Fluent report writing in English

- Strong computer literacy, including well-developed computer skills in applicable software

- Ability to work independently and effectively prioritize tasks

## Skills

### Required
- clinical research
- data analysis
- medical terminology
- GCP
- FDA regulations
- report writing
- communication skills

### Nice to have
- clinical/project management

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Source: [Apply at iqvia.wd1.myworkdayjobs.com](https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Taipei--Taipei-City-Taiwan/XMLNAME-18287-Assoc-Patient---Site-Svcs-Mgr_R1232926?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply)