Kamila Laskowska

Coordinated global clinical trials, ensuring timelines, quality, and regulatory compliance. Managed eTMF activities, QC, and inspection readiness in Veeva Vault. Collaborated with CROs, vendors, and cross-functional teams. Developed Power BI/Veeva dashboards to track study progress, metrics, and risks. Managed trial finance, POs, invoices, insurance documentation, and renewals. Supported data quality checks, CTMS updates, validation activities, and study reporting.

CTA: Maintenance of documents in eTMF and CTMS (Veeva). Document management of clinical studies in compliance with GCP and relevant SOPs. Support of Clinical Project Managers with invoice management. Preparation, review and maintenance of SOPs, communication with CRO, vendors and sites. QA: Conducting Quality Control checks on 12 studies in order to ensure that data and documents are accurate, complete, and consistent. Data Management: Development of dashboards - creation interactive display of data in cat

Administrative support: Maintaining global communication and coordination with all company's units regarding service and changes for global processes. Data Management: Update of site information in internal software. Database checks and data revision performance. Creation and maintaining CTMS trackers.

Project of supporting the data migration into the new database, in order to store master data related to the pharmaceuticals and health technology products associated with treatment of HIV, Tuberculosis, and Malaria. Ensuring that all data is accurately and completely migrated from legacy systems, tools and tables. Reconciliation of data across different data sources are unstructured.

Providing a review of clinical trial data, as a result of the impact of COVID-19 to onsite monitoring visits: performing trend analysis and investigation of potential risks. Surveillance of Key Risk Indicators at a trial level. Spot checks of monitoring visit reports. Proactive support of Central Monitoring Managers. Maintenance of global communication.

Generate daily reports concerning step of fermentation process, determining level of diacetyl and viability of yeast, checking contamination of tanks, verifying correctness of the beer aging process, dry hops sterilization, checking can seams, basis weight, oxygen and carbon dioxide level during canning process.

Participant of trainings on the subject of clinical trials, such as medical documentation in a clinical trial, GCP, Safety reporting AE/SAE, Start-up process and contracting of research sites. Application of the systems e.g. CTMS, CTP, eTMF.

Duties include familiarizing guests with menu and daily specials, accurately recording food and drink orders, running multi-course meals, and tallying bills.

Analysis of properties of gluten-free bread, testing the elasticity, water absorption, expiration date and the impact of bread storage in various conditions.

Being responsible for the management of knowledge, coordinating trainings and meetings, responsible for recruitment process, motivation, gratification, and overall human resources in local BEST group, being involved in international representation of BEST Lodz and general development of association.

Specialization: Applied Biotechnology in English Thesis: "The study of alloyed nanoparticles of noble metals as glucose oxidase and catalase mimetics"

Specialization: Technical Biochemistry Thesis: "Biosolubilization of brown coal with the participation of candida Tropicalis"