Marta Puchała

Experience

• 

  National Institute of Public Health, Poland

  Jul 2018 - Sept 2018

  Student Intern
• 

  Laboklin Polska Sp. z o.o.

  Dec 2018 - Nov 2020

  Laboratory Worker / Accredited Specialist Laboratory for Veterinary Diagnostics, Polish Branch

  - Analysis in the field of laboratory diagnostics - hematology (examination of blood smears), clinical chemistry, endocrinology, serology researches (IFAT, ELISA), urinalisys with sediment, another diagnostic auxiliary tests- Using of laboratory equipment, controlling and conservation- Evaluating, assessment and description medical samples according Mecical Literature & knowledge

• 

  Biokinetica

  Dec 2020 - Dec 2021

  Laboratory Coordinator Assistant / Laboratory of Early Phase Institute

  - Processing of medical samples (blood & urine) according required Clinical Trial Protocols,- Working with medical documentation, completion and management of Logs, patient‘s cards and tests results- Packing & forwarding samples to partner diagnostic laboratories & Sponsor’s dedicated Laboratories- Support for Clinical Researches activities performed at the Institute- Cooperation with internal departments, Clinical Trial’s Bodys and external partners involved in Researches- Taking part in Clinical Researches Participants and Patients visits via taking care of taken samples- Taking part in internal audits, self QC and compliance ensuring Sponsor’s Instructions & SOPs Show less

• 

  Pfizer

  Jan 2022 - Feb 2024

  - Review and interpret the data provided by Regulatory Strategists to establish systems & tools required to be populated in line with current standard operating procedures, WI & SOPs- Perform data entry and quality control tasks associated in all global regulatory systems impacted- Regulatory Data Entry and EndToEnd Archive Process- Creating and maintaining registrations within the system ; updates include: MAA numbers, Renewals, Lifecycle, Withdrawals, Launches, Discontinuations- Initializing Query Workflow- Archiving Correspondence Documents between the Agency and Company- Support global/local team members with data management workload- Being Point of Contact fo Regional Strategists from difference Markets - providing solutions how -country specifics should be tracked within the system according to the current SOPs/WIs; act as Regulatory Data SME in AfME- Adhering to quality control procedures and standards ensuring Regulatory Compliance- Support audit as part of regulatory data/system scope- Management of Data of Acquisition Product, Covid-19 associated Products and Clinical Trials Applications- Participation and being representative by Department in Company’s Projects at global level- Training of new hires & support Team environment in daily work Show less

  • Data Associate

    Feb 2023 - Feb 2024

  • Junior Data Associate

    Jan 2022 - Jan 2023
• 

  ICON plc

  Mar 2024 - now

  Clinical Trial Assistant