Experience

European Society of Anaesthesiology and Intensive Care

• Belgium
• Medical Practices
• 1 - 100 Employee

• Clinical Trial Assistant

  • Jun 2021 - Present



IVECO

• Italy
• Motor Vehicle Manufacturing
• 700 & Above Employee

• Product and customer support administrator

  • May 2021 - Jun 2021



Viessmann

• Renewable Energy Semiconductor Manufacturing
• 700 & Above Employee

• Administrative Assistant

  • Aug 2020 - Dec 2020

  Preparing and making quotes for solar panels. Informing the clients by telephone/email Preparing and making quotes for solar panels. Informing the clients by telephone/email



ERT

• United States
• Pharmaceutical Manufacturing
• 700 & Above Employee

• Lead Data Coordinator Respiratory

  • Sep 2017 - Jun 2020



Biomedical Systems

• United States
• Pharmaceutical Manufacturing
• 100 - 200 Employee

• Project Assistant

  • Aug 2016 - Sep 2017

  - Review daily workload of data coordinators and assist if needed- Assist in updates of study documents - Distribute Status Reports to study team members - Complete order form requests- Assist with training of new employees- Assist in edit check review in the pulmonary database - Assist with data reconciliation and error listings- Perform other duties as deemed necessary to maintain the highest quality service

• Data Specialist ABPM, holter, cardiac, respiratory, TTM

  • Jun 2004 - Aug 2016

  - Knowledgeable of Protocol specific Processing Instructions.- Provide customer service to the investigative sites, CRO or Sponsor as needed.- Provide technical support for daily incoming calls or delegate to the appropriate person/division.- Review daily transmission for completeness and consistency according to the Sponsor Protocol.- Accountable for the verification of all data entry for patient demographic information.- Verify and document any necessary changes due to the discrepancies. Notify the appropriate investigative site of any discrepancies noted (i.e. issue queries).- Identification of all reports that meet Protocol specific verbal and non verbal alert criteria.- Distribute final reports and alert reports to investigative sites/Sponsors/CROs as needed.- Interface with Data Management regarding the submission of data.- Knowledgeable of job related SOPs,- Visually verify and approve all manually entered information of clinical data- Visually verify and approve all entered values in the supplemental databases Show less



N-Allo

• Mechelen

• Clients advisor

  • Nov 2003 - May 2004



Scoot

• Grimbergen

• Executive customer service

  • Jul 1998 - Mar 2002