Iris Tauscher Email & Phone Number

Leipzig Und Umgebung

• Leading cross-functional teams through global improvement / transformation programs
• Tactical and strategic planning with functional stakeholders as well as partnering and consulting to ensure the establishment of a continous improvement culture and delivery of customer value and financial business.
• Onboarding and people development / management for the business transformation team

München Und Umgebung, Deutschland

• Lead and manage the dynamics of cross-functional process improvement projects and business-wide transformation initiatives including training, mentoring, and consulting.
• Responsible for assessing existing business processes and implementing streamlined, efficient and consistent solutions globally throughout the organization using PM, Six Sigma and Lean methodology.
• Leading and overseeing acquisition and integration efforts

Leipzig Und Umgebung, Deutschland

🔹 As third rotation I moved into a Process Management Role to identify, execute and manage process improvement opportunities. I was leading an initiative for more effective and globally harmonized SOP Management and also acted as SOP Liaison providing oversight and process ownership for Clinical Operations SOPs.

Leipzig Und Umgebung, Deutschland

I continued with supervision and management of Direct Reports in ClinOps and Start-up. The year 2013 brought an exciting change to my career development as I was invited to join the Management Development Program (MDP) on a three year rotation. 🔹In my first rotation (Oct 2013 - Jul 2014), I was responsible to facilitate and support the implementation of.

Leipzig Und Umgebung, Deutschland

I moved from my SCRA role with partly Line Management into a full Line Management role and took care for Direct Reports in ClinOps and Start-up across Germany, Austria and Switzerland, including all aspects of Performance Review and Management as well as conduct of Quality Control and Evaluation Visits.

Dresden Und Umgebung, Deutschland

I continued to work in the role of a Senior Clinical Research Associate with Site Management and Site Monitoring responsibilities with Sites in Germany as well as Austria. In addition to that I started with Line Management activities for junior CRAs in May 2008.

Dresden Und Umgebung, Deutschland

I started to work homebased for a Clinical Research Organization with it's German Office in Munich. My main responsibilities as CRA II were all kinds of site visits (from Pre-Study to Close-out), Processing of Site Payments and Support for Regulatory Submissions. I was also acting as a Lead CRA for a Dyslipidemia trial during that time.

Dresden Und Umgebung, Deutschland

I got the opportunity to act as Study Nurse in the SMO organization of the company. This did include maintenance and completion of Patient Files and Case Report Forms, support for Physical Patient Examinations as well as Lab sample processing and shipments.

Dresden Und Umgebung, Deutschland

This role combined Clinical Operations- with Start-up Activities. I performed Site Selection-, Pre-Study-, Initiation-, Close-out as well as regular Monitoring Visits. I continued to support and prepare local and national regulatory submissions as well as Trial Documentation Maintenance.

Dresden Und Umgebung, Deutschland

My entry position into clinical research at a Clinical Research Organization (CRO) headquartered in Dresden, Germany. I was responsible for Document and Data Management (Trial Master file Maintenance), supporting Clinical Research Associate (CRA) and Project Management (PM) activities and preparing onsite visits as well as assisting with regulatory.