# Regulatory Team Leader

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

**Apply**: https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Osaka-Japan/Reg-Affairs-Mgr_R1574062-1?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/jobs/job_a0da16d1-58b

## Description

We are seeking a Regulatory Team Leader to work independently under limited supervision on complex projects. You will act as a Regulatory Team Leader, write regulatory and technical documents, establish relationships with customers, and undertake detailed review and management of budgets.

Responsibilities:

- Act as a Regulatory Team Leader on complex projects

- Write regulatory and technical documents with minimal review by senior staff

- Establish relationships with many customers and discuss regulatory issues

- Undertake detailed review and management of budgets related to projects

- Give guidance to junior colleagues and assist in their training and development

- Present to clients at bid defense meetings

- Write new regulatory standard operating procedures and propose revisions

- Perform other tasks or assignments as delegated by Regulatory management

Requirements:

- Bachelor's or Master's Degree in Life Science or related discipline

- At least 8 years of relevant experience

- Good understanding of the Research and Development process, laws, and related guidelines

- Specific regulatory or technical expertise

- Expert in planning and delivering work on time with quality parameters in mind

- Knowledge of regulatory procedures in the appropriate region

- Good working knowledge of regional regulatory intelligence

- Ability to work closely with client regional heads and establish effective working relationships

- Strong software and computer skills, including Microsoft Office and publishing applications

- Ability to work on several projects with direction from senior staff

- Ability to follow standard operating procedures consistently and provide independent thought

- Advanced knowledge within a specific discipline typically gained through extensive work experience and/or education

## Skills

### Required
- Life Science
- regulatory affairs
- project management
- budget management
- Microsoft Office

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Source: [Apply at iqvia.wd1.myworkdayjobs.com](https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Osaka-Japan/Reg-Affairs-Mgr_R1574062-1?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply)