Robert Gall Email & Phone Number

Berlin, Germany

- Clinical trial management and coordination- Contract & budget negotiation- Audit preparation- Preparation of study specific documents and source data (worksheets)

Berlin, Germany

Managing international clinical studies of phase II & III in dermatology as local and as global project manager

Berlin, Germany

Local Submissions Specialist who prepares ongoing submissions, amendments and periodic notifications required by central and local EC and RA and other local regulatory authorities as needed in Germany and Austria

Berlin Area, Germany

Main contact for CROs and sponsors; deputy head of the own trial center (main focus: dermatology); line management & training of the Study Nurses and Study Coordinators; coordination of resources & supplies; budget negotiation and control; quality control; feasibility support; submissions preparation; development of study specific source data; monitoring & audit support, medical photography

Berlin Area, Germany

Managing phase I and IIa clinical studiesManaging of study teams and CROs; development of protocols, ICFs and EC/IRB submission documents; budget planning and control; lead CRA for my studies

Berlin Area, Germany

EC submission preparation, development of study specific source data, coordination of resources and supplies, guidance to study nurses and investigators, quality control, monitoring support, audit preparation, safety reporting, medical photography, maintenance of the archive

Berlin Area, Germany

Planning, coordination & management of phase III trials in Russia and Central Eastern Europe: Main contact for CROs and vendors; submission preparation; monitoring control; contract and budget negotiation and control; management of IMP supply; medical writing

Bad Vilbel, Germany

Preparation of dossiers for generics applications in Western Balkan & Asia, coordination of the application process, change control procedures, key user for the regulatory data base Register & document management system CSC FirstDoc

Darmstadt Area, Germany

- preparation and maintenance of Trial Master Files- conception of TMFs, investigator files and study documents for sponsors and internal use- assistance to the project managers and CRAs (study team communication, meetings, payments, documentation)- occasional co-monitoring

Bad Homburg, Germany

Professional training in medical documentation with main focus on clinical research as well as 1.5 years of inhouse training and work as CTA & clinical monitor.

Ausbildung / Professional Education, Media And Information Services – Medical Documentation

Biology, General