Robert Gall

Robert Gall Email and Phone Number

Clinical Project Manager @ VOIANT℠
Robert Gall's Location
Berlin, Berlin, Germany, Germany
Robert Gall's Contact Details

Robert Gall work email

Robert Gall personal email

n/a
About Robert Gall

An experienced clinical research manager and consultant with in depth knowledge from the sponsor, CRO and trial center side. Since 2006 participation in more than 115 clinical studies from phase I to IV, of which more than 80 were dermatology studies. Management of phase I, II & III studies since 2017.

Robert Gall's Current Company Details
VOIANT℠

Voiant℠

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Clinical Project Manager
Robert Gall Work Experience Details
  • Voiant℠
    Clinical Project Manager
    Voiant℠ Nov 2024 - Present
    Berlin, Germany
  • Freelance
    Clinical Research Consultant
    Freelance Jul 2024 - Present
    - Clinical trial management and coordination- Contract & budget negotiation- Audit preparation- Preparation of study specific documents and source data (worksheets)
  • Symbio Proinnovera
    Clinical Project Manager
    Symbio Proinnovera Nov 2022 - Jun 2024
    Berlin, Germany
    Managing international clinical studies of phase II & III in dermatology as local and as global project manager
  • Syneos Health
    Site Start-Up & Regulatory Specialist Ii
    Syneos Health Jul 2022 - Oct 2022
    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
  • Isa - Interdisciplinary Study Association Gmbh
    Study Manager
    Isa - Interdisciplinary Study Association Gmbh Jun 2018 - Jul 2022
    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
  • Bayer Via Hays Professional Solutions
    Study Manager
    Bayer Via Hays Professional Solutions Aug 2017 - May 2018
    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
  • Study Center Of Dermatology Practice Dres. Scholz, Sebastian, Schilling
    Clinical Study Coordinator
    Study Center Of Dermatology Practice Dres. Scholz, Sebastian, Schilling Aug 2013 - Jul 2017
    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-Chemie Ag
    Clinical Trial Coordinator
    Berlin-Chemie Ag Sep 2011 - Aug 2013
    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
  • Stada
    Regulatory Affairs Assistant
    Stada Oct 2010 - Aug 2011
    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
  • Premier Research
    Clinical Trial Associate Ii
    Premier Research Feb 2009 - Sep 2010
    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
  • Chiltern International
    Apprenticeship: Specialist In Media & Information Services - Medical Documentation
    Chiltern International Sep 2006 - Jan 2009
    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.

Robert Gall Skills

Clinical Trials Gcp Regulatory Affairs Ctms Clinical Monitoring Regulatory Submissions Ich Gcp Clinical Research Good Clinical Practice

Robert Gall Education Details

Frequently Asked Questions about Robert Gall

What company does Robert Gall work for?

Robert Gall works for Voiant℠

What is Robert Gall's role at the current company?

Robert Gall's current role is Clinical Project Manager.

What is Robert Gall's email address?

Robert Gall's email address is ro****@****mail.de

What schools did Robert Gall attend?

Robert Gall attended Ihk / Chiltern, Ernst-Moritz-Arndt-Universität Greifswald.

What skills is Robert Gall known for?

Robert Gall has skills like Clinical Trials, Gcp, Regulatory Affairs, Ctms, Clinical Monitoring, Regulatory Submissions, Ich Gcp, Clinical Research, Good Clinical Practice.

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