GV Medical Research and Consultancy
o To ensure that Investigators are conducting clinical trials in accordance with international Regulatory and Ethical guidelines for ICH - GCP.
Bedrijfsgegevens
Bedrijfsnaam: GV Medical Research and Consultancy
Naam: Lieve Vrints
Vestigingsplaats: WAUBERG-PEER, BE
Actief sinds: 09-01-2017
Clinical Research Associate
To ensure that Investigators are conducting clinical trials in accordance with international Regulatory and Ethical guidelines for ICH - GCP. Participation in the study development and start-up process including reviewing protocols, drafting Monitoring Plan, reviewing CRF’s during development process, preparation of Informed Consents, developing study specific documents, translations of study critical documents, presenting at Investigator Meetings, developing project specific CRA training. Contract and budget negotiations, technical, educational and clinical support. Conducting Site selection – initiation – training – monitoring – close out visits. Coaching – QA assessment visits. Translations Eng-Fr-Nl. Medical secretary.