Języki
angielski
biegły
Doświadczenie zawodowe
Research Coordinator (Inhouse Monitor, Inhouse CRA)
International, multicenter trial, III phase, international team.
Responsible for Polish sites:
-verifying that investigators follow the approved protocol and GCP procedures,
-checking that SAEs are reported on time and according to procedures,
-monitoring that trial data are reported in study systems wihin agreed timelines, that are complete and accurate;
-encouraging investigators to achieve their recruitment targets;
-ongoing help to investigators;
-close cooperation with CRAs;
-management of clinical trial documentation and systems;
-handling of investigators payments;
-assistance in organization of Investigator Meetings;
-Cooperation with other parties.
Responsible for Polish sites:
-verifying that investigators follow the approved protocol and GCP procedures,
-checking that SAEs are reported on time and according to procedures,
-monitoring that trial data are reported in study systems wihin agreed timelines, that are complete and accurate;
-encouraging investigators to achieve their recruitment targets;
-ongoing help to investigators;
-close cooperation with CRAs;
-management of clinical trial documentation and systems;
-handling of investigators payments;
-assistance in organization of Investigator Meetings;
-Cooperation with other parties.
CTA / CTA to CTL & PM / Project Associate
International, multicenter trials.
-Cooperation with study Team, the Sponsor and other parties.
-Organization of teleconferences (with study Team, the Sponsor, other parties) and writing minutes from them.
-Maintaining the tracking systems for study data.
-Reporting of study progress the Sponsor.
-Updating of study procedures and forms and distribution them to study Team.
-Preparing study documentation for archiving (for the Sponsor and locally).
-Organization of Investigator Meetings.
-Management of clinical trial documentation.
-Cooperation with study Team, the Sponsor and other parties.
-Organization of teleconferences (with study Team, the Sponsor, other parties) and writing minutes from them.
-Maintaining the tracking systems for study data.
-Reporting of study progress the Sponsor.
-Updating of study procedures and forms and distribution them to study Team.
-Preparing study documentation for archiving (for the Sponsor and locally).
-Organization of Investigator Meetings.
-Management of clinical trial documentation.
Edukacja
Specjalizacje
Badania i rozwój
Farmaceutyka/Biotechnologia
Zainteresowania
Irish music, Agatha Christie, yerba mate.
Inne
Husband and two daughters (4 and 9).
Grupy
Clinical Research & badania medyczne
Grupa dla wszystkich badaczy, lekarzy, naukowców i ludzi biznesu związanych pośrednio i bezpośrednio z medycyną
Klub Miłośników Yerba Mate
Forum dla luźnych dyskusji sprowokowanych przez siorbanie lub podczas siorbania wymienionej w tytule.
Uniwersytet Kardynała Stefana Wyszyńskiego w Warszawie
Uniwersytet Kardynała Stefana Wyszyńskiego w Warszawie