# Associate Director, Biostatistics

**Company**: IQVIA
**Work arrangement**: hybrid
**Experience**: senior
**Job type**: permanent
**Category**: Data Science
**Industry**: Healthcare

**Apply**: https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Frankfurt-Hesse-Germany/Associate-Director--Biostatistics---Global-BIOS_R1275565?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
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## Description

We are seeking an Associate Director, Biostatistics to join our award-winning and innovative department at IQVIA. As a member of the Global Biostatistics team, you will have the opportunity to work globally and across a variety of therapeutic areas.

The Global Biostatistics team at IQVIA is experienced in submissions for all major regions and works closely with key groups such as Global Regulatory Affairs, Safety, Project and Data Management, and Medical Writing to drive efficiency and accountability.

As an Associate Director, Biostatistics, you will manage a team of Biostatistics staff and serve as a site head or functional head within a site. Your responsibilities will include:

- Providing direction and guidance in carrying out project assignments

- Interfacing with clients and other internal departments

- Applying advanced statistical methods to project work

- Serving as a resource for the department to ensure scientific integrity in the application of statistical methodology to clinical trials

- Assisting the Director in strategic planning and resource allocation for the department

- Participating in oversight across studies and/or customers, including guidance on documentation and output development/review

- Assisting the Director in proposal development, project allocation, budget projections, and client presentation, as needed

To be successful in this role, you will need:

- A BSc or MSc degree in Biostatistics or a related field

- 10+ years of relevant experience within the life-science industry, with at least 2 years of experience in managing staff

- Familiarity with complex statistical methods that apply to Phase I-IV clinical trials

- In-depth knowledge of applicable clinical research regulatory requirements, such as Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines

- Strong working knowledge of SAS

- Working knowledge of relevant Data Standards, such as CDISC/ADaM

In return for your hard work and dedication, we offer:

- Global exposure

- Variety of therapeutic areas

- Collaborative and supportive team environment

- Access to cutting-edge in-house technology

- Excellent career development and progression opportunities

- Work-Life Balance

## Skills

### Required
- Biostatistics
- Statistical methods
- SAS
- CDISC/ADaM
- Good Clinical Practice (GCP)
- International Conference on Harmonization (ICH) guidelines

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