Anna Szymczyk Email & Phone Number

Łódź, Pl

Warszawa, Woj. Mazowieckie, Polska

Management of a single adverse reaction case including coding according to MedDRA terminology, follow-up, reporting to EU and non-EU AgenciesPerforming ICSR download operationsPerforming reconciliation process with partners,Entering drug product data into the xEVMPD product database and updating it on an ongoing basisRegistration of responsible parties in the EudraVigilance databasePreparation of reports on the signal detection process

Warszawa, Woj. Mazowieckie, Polska

Performsing Sponsor Data Entry as applicable per data management plans following entry guidelines;Runs data integrity check reports in accordance with data review plans and relevant SOPs;Raising questions to investigational site staff;Assists the CDM/SCDM/LCDM with data management activities to ensure all identified data issues are resolved prior to study database lock;May temporary support other E2E Data Management activities under the guidance of the CDM/SCDM/LCDM of the trial if defined as needed;Assists the CDM/SCDM/LCDM during Trial Start-up phase;Assists the CDM/SCDM/LCDM to prepare metrics at study level.

Łódź, Woj. Łódzkie, Polska

Providing pharmacutical care for patientsFilling prescriptionsPerforming duties with respect for pharmacutical lawOrdering goods

Łódź, Woj. Łódzkie, Polska

account: "umed_oczamistudenta"Social media managementContent creationMonitoring and analysis of resultsVideo recording and editingTrend analysis

Łódź, Woj. Łódzkie, Polska

Conducting clinical trialsParticipation in the clinical trials procurement process Feasibility fulfillmentTraining the research team in clinical researchCoordinating clinical trials at site levelMaintenance of study documentation (e.g. ISF, study logs) Planning and controlling the implementation of patient visit proceduresPreparing documentation for clinical trialsVerifying the completeness of patient medical records (in the context of clinical trial requirements)timely input of data into IT systems (e.g. eCRF)Cooperation with clinical trial monitors and investigators Cooperation with patients included in clinical trials

Łódź, Woj. Łódzkie, Polska

Assisting in the preparation of cytotoxic drugs Assisting in the preparation of parenteral nutrition for children and adultsAssistance in preparation of tendersCalculating dosages of drugs and nutritions individually for patients

Łódź, Woj. Łódzkie, Polska

Administrative and office workOperation of the OfficeOperation of the UMED recruitment IT system Receiving and verifying candidates' documents Day-to-day contact with the candidate