Oferty dla Protocol praca Polska

01.01.2012 | Pełny etat | Małopolskie | Hays PolandAccording to Standard Operating Procedures and GCP Guidelines Experience - Skills Required · Minimum of 3 years of clinical research monitoring experience · Ability to monitor study sites independently according to protocol monitoring guidelines, S.O.P.s, GCP. · Experience in cardiology essential · Good

01.01.2012 | Pełny etat | Warszawa | Hays PolandAnalysis of test results and reporting within test protocol forms respectively acceptance protocols for the tests and test stages - Assistance for commissioning activities

01.01.2012 | Pełny etat | Mazowieckie | Hays PolandData are correct, complete and verifiable by comparing with the original documents. Furthermore, it is a responsibility of the SCRA to assure that the clinical trial is being performed according to the valid trial protocol, amendments, ICH-GCP guidelines and legal regulations in force. The SCRA

01.01.2012 | Pełny etat | Hays PolandOraz rekrutacja badaczy - wypełnianie odpowiedniej dokumentacji o statusie badania (study status report) - dostarczenie na czas odpowiedniej dokumentacji do komisji etycznej (protocol/consent documents/safety reports)

01.01.2012 | Pełny etat | Mazowieckie | Hays PolandAre protected, and that the reported data are correct, complete and verifiable by comparing with the original documents. Furthermore, it is a responsibility of the SCRA to assure that the clinical trial is being performed according to the valid trial protocol, amendments, ICH-GCP guidelines and legal

01.01.2012 | Pełny etat | Hays PolandEmbedded Software Engineer Location Poland Responsibilities - Embedded software development for drivers, protocol stacks and applications - Digital TV and STB development - Integration and testing of systems - UML

01.01.2012 | Pełny etat | Mazowieckie | Hays PolandWypełnianie odpowiedniej dokumentacji o statusie badania (study status report) - dostarczenie na czas odpowiedniej dokumentacji do komisji etycznej (protocol/consent documents/safety reports)

01.01.2012 | Pełny etat | Mazowieckie | Hays PolandSelecting, initiating and close-out of appropriate investigational sites for clinical studies and monitoring those sites in order to ensure that studies are carried out according to the study protocol and in accordance with client SOPs, applicable regulations and the principles of ICH -GCP