Associate Director Biostatistics - Global BIOS

Associate Director Biostatistics Permanent w / m / d

Global Biostatistics

HomeBased / Hybrid : Germany

Join us on our exciting journey!

The Global Biostatistics (Data Sciences Safety & Medical) team at IQVIA are experienced in submissions for all major regions; working together with key groups such as Global Regulatory Affairs Safety Project and Data Management and Medical Writing to drive efficiency and accountability.

We have one of the largest Biostatistics departments within the industry of around 1100 staff to which we engage the full range of industryleading resources and expertise spanning all study phases and therapeutic areas.

Due to continued growth we are seeking new brave minds to join our award winning and innovative department. You will have the opportunity to work globally and across a variety of therapeutic areas.

IQVIA Biostatistics helps interpret and draw inferences from data collected on patients as they progress through a clinical trial and serves as the bridge between data capture and reporting.

Job Overview :

As an Associate Director Biostatistics with regional / site presence you will manage a team of Biostatistics staff and fulfil the role of site head or functional head within a site.

You will provide direction and guidance in carrying out project assignments interfacing with clients and other internal departments and applying advanced statistical methods to project work.

Coupled with serving as a resource for the department ensuring scientific integrity in the application of statistical methodology to clinical trials and assist the Director in strategic planning and resource allocation for the department.

You will also participate as oversight across studies and / or customers including guidance on documentation and output development / review and assist the Director in proposal development project allocation budget projections and client presentation as needed.

Requirements :

BSc or MSc degree in Biostatistics or related field and 10 years relevant experience within the lifescience industry along with at least 2 years experience in managing staff

Familiarity with complex statistical methods that apply to Phase IIV clinical trials

Indepth knowledge of applicable clinical research regulatory requirements i.e. Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines

Familiarity with moderately complex statistical methods that apply to applicable clinical trials

Strong working knowledge of SAS

Working knowledge of relevant Data Standards (such as CDISC / ADaM)

From camaraderie to professional development working at IQVIA provides unique opportunities to advance your career alongside a group of diverse and talented colleagues.

What is in it for you

Global exposure

Variety of therapeutic areas

Collaborative and supportive team environment

Access to cuttingedge inhouse technology

Excellent career development and progression opportunities

WorkLife Balance

JOIN US

Embrace your curiosity and grow your career in an exciting environment where development is a priority.

Think boldly and disrupt conventional thinking.

Enjoy what you do.

Whatever your career goals we are here to ensure you get there!

IQVIA is a leading global provider of advanced analytics technology solutions and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible to help our customers create a healthier world. Learn more at

Required Experience :

Exec

Key Skills

Program assessment,FDA Regulations,Manufacturing & Controls,Program Evaluation,budget forecast,Research Experience,Operations Management,Research & Development,Strategic Planning,Contract Management,Leadership Experience,negotiation

Employment Type : Full-Time

Experience : years

Vacancy : 1