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Sponsor Oversight

GWT: Your independent sponsor for comprehensive clinical trials

Die GWT — your partner as an independent clinical sponsor for comprehensive clinical trials

GWT - Society for Knowledge and Technology Transfer is your reliable partner in the field of Sponsor Oversight and independent, clinical sponsor for Investigator Initiated Trials (IIT studies), Medicines Act (AMG) studies, Medical Devices Act (MPG) studies and Non-Interventional Studies (NIS) studies. As a service provider, we are responsible for your clinical trials and research projects.

Your benefits at a glance

Over 25 years of experience in international, multi-site clinical trials of diverse medical indications.
Extensive expertise and quality in hematology, oncology, immunotherapy, pneumology and more.
Efficient, cost-effective access to patient populations through European trial site network.
Expert teams in project management, safety/PV, data management, monitoring, regulatory affairs and administration.
Smooth, professional implementation of your clinical trials through expert support.

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GWT - your innovation through expertise and network in clinical research

Working with GWT means that you will benefit from our many years of experience and our extensive network. We always strive to meet your requirements in the best possible way and to develop innovative solutions that meet current and future clinical research requirements.

GWT - Your trusted partner for groundbreaking success in clinical research

Trust GWT as your partner for sponsor oversight and independent sponsor in clinical research. Together, we will set new standards and work hand-in-hand for the success of your clinical trials.

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Sponsor oversight with GWT experts

Dr. Werner Joachim Bokranz

Clinical Data Manager

Phone:
+49 351 25933 283

Email:
werner.bokranz@g-wt.de

Petra Gerteis

Clinical Safety Specialist

Phone:
+49 351 25933 124

Email:
petra.gerteis@g-wt.de

Monica Johanna Gomez Sarmiento

Clinical Project Assistant

Phone:
+49 351 25933 191

Email:
monica.gomez@g-wt.de

Dr. Linda Hein

Clinical Monitoring Specialist

Phone:
+49 351 25933 179

Email:
linda.hein@g-wt.de

Franziska Hoppe

Team Leader Clinical Monitoring

Phone:
+49 351 25933 180

Email:
franziska.hoppe@g-wt.de

Dr. Carsta Köhler

Scientific Head of Medical Department

Phone:
+49 351 25933 190

Email:
carsta.koehler@g-wt.de

Wera Kupetz

Team Leader Clinical Safety

Phone:
+49 351 25933 173

Email:
wera.kupetz@g-wt.de

Dr. Katrin Linke

Clinical Project Manager

Phone:
+49 351 25933 176

Email:
katrin.linke@g-wt.de

Nathalie Pfeiffer

Clinical Monitoring Specialist

Phone:
+49 351 25933 167

Email:
nathalie.pfeiffer@g-wt.de

Jana Plätschke

Senior Clinical Regulatory Specialist

Phone:
+49 351 25933 126

Email:
jana.plaetschke@g-wt.de

Dr. Anna Polowinski

Clinical Project Manager

Phone:
+49 351 25933 171

Email:
anna.polowinski@g-wt.de

Martin Puttrich

Team Leader Clinical Quality Management and Process Digitization

Phone:
+49 351 25933 193

Email:
martin.puttrich@g-wt.de

Bukuri Qoqaj

Clinical Project Assistant

Phone:
+49 351 25933 282

Email:
bukuri.qoqaj@g-wt.de

Corina Röllig

Clinical Data Manager

Phone:
+49 351 25933 174

Email:
corina.roellig@g-wt.de

Dr. Arnold Schröder

Team Leader Clinical Project Management Office Berlin

Phone:
+49 351 25933 241

Email:
arnold.schroeder@g-wt.de

Dr. Michael Teubner

Senior Clinical Monitor

Phone:
+49 351 25933 244

Email:
michael.teubner@g-wt.de

Dr. Michael Unger

Team Leader Clinical Data Management

Phone:
+49 351 25933 181

Email:
michael.unger@g-wt.de

Dr. Carmen Weigt

Senior Clinical Project Manager

Phone:
+49 351 25933 172

Email:
carmen.weigt@g-wt.de

Ina Wendler

Clinical Project Assistant

Phone:
+49 351 25933 240

Email:
ina.wendler@g-wt.de

Dr. Regina Willecke-Hochmuth

Clinical Monitoring Specialist

Phone:
+49 351 25933 170

Email:
regina.willecke-hochmuth@g-wt.de

Dr. Ines Winkler

Clinical Project Manager

Phone:
+49 351 25933 188

Email:
ines.winkler@g-wt.de

GWT: Your independent clinical sponsor partner for research excellence and customized solutions

GWT - Your experts for ICH-GCP compliant sponsor tasks: Comprehensive expertise and prudent strategies to ensure patient safety, data integrity and efficient risk management in clinical trials. Rely on over 25 years of experience and our dedicated teams.

Clinical Monitoring

Our experienced CRA team and nationwide network ensures comprehensive support in hematology, oncology, diabetes, dermatology, pulmonology and cardiology. We guarantee ICH-GCP-compliant monitoring, patient safety, high data quality and compliance with test plans and laws.

Clinical Safety

Our expertise in IITs, NIS and PASS studies ensures seamless recording and reporting of SAEs, and early risk identification and transparent communication. Our experienced team and network ensures patient safety and data integrity according to ICH-GCP guidelines - for successful studies.

Clinical Study Design Advice

Support for clinical trials (Phase I-IV), non-interventional studies, scientifically initiated studies, Medical Device Act studies and market approval studies. GWT offers long-standing expertise in patient and study site planning for multicenter/multinational projects with a specialization in hematology, oncology, pulmonology, dermatology and ophthalmology.

Preclinical Study Advice

GWT supports you in experiment design, statistical analysis, pharmacology, toxicology, GMP manufacturing, analytics, scientific advice (PEI, BfArM) and scientific writing. Benefit from our expertise in preclinical advice, regulatory requirements (EMA, FDA). We support you in experiment design, statistical analysis, pharmacology, toxicology, GMP manufacturing, analytics, scientific advice (PEI, BfArM) and scientific writing.

Thank you for your interest in our services. We gladly answer your enquiries!

Dr. Carsta Köhler

Scientific Head of Medical Department

Phone:
+49 351 25933 190

Email:
carsta.koehler@g-wt.de

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Clinical Trials

Strategic Management

Sponsor Oversight
GWT: Your independent sponsor for comprehensive clinical trials

Clinical Project Management
Comprehensive coordination of all aspects of your clinical trial

Clinical Project Administration
Seamless communication and administration of your clinical trial

Clinical Data Management
Ensuring the highest quality and 100% integrity of your clinical data

Clinical Quality Management
Highest quality standards in the supervision of your clinical trial

Clinical Safety

Clinical Monitoring

Study Promotion

Preclinical Advice

Study Design Advice

Real World Data Sets

GWT StudyDesigner

Transform your study design with GWT StudyDesigner - Real-time interactive design and expert advice for your clinical research!

Industry Projects

Strategic Consulting

Project Administration
Efficient administrative implementation of industrial projects

Contract Management
Individual consulting for legally compliant transfer projects

Financial Management
Ensuring and carrying out correct financial transactions

Human Resources Management

Infrastructure Management

Startup Backoffice

Turn your ideas into action - supported by GWT's comprehensive business platform.

Are you ready to become entrepreneurial and focus on your product?

Take on the role of project manager and act like an entrepreneur while we support you

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