Description de l'emploi
Primary responsibility for managing and developing the Corporate Drug Safety, Medical Safety Evaluation Group.
Review and coordinate medically appropriate evaluation of Signal management, safety risks and benefit-risk assessments of Medical Safety Evaluation assigned product portfolio in all stages of marketing or development and Europe and international.
Cooperate providing SPC, PBRER, RMP, Development study safety profile,- DSUR, Clinical trials protocols, SAP, Clinical study reports, Clinical overview, PIP, Investigator brochure and ICF.
In cooperation with the QPPV Head responsible for the coordination of Medical Safety Evaluation related medical crisis management;
Coordinate and define Corporate Drug Safety Evaluations Processes;
Manage staff and budget planning of Corporate Drug Safety;
Possibility for career progression is assumed for the right individual
Recruitment for this role is managed by Sr Consultant Vladyslav Babych, for more information and confidential discussion please apply and /or call to Volt Europe office
