Job Description
• Clinical research initiation and coordination;
• selection of research centers;
• initial submission for regulatory institutions;
• monitoring of research process;
• preparing documents and reports.
• selection of research centers;
• initial submission for regulatory institutions;
• monitoring of research process;
• preparing documents and reports.
Requirements
• Higher education in a scientific or healthcare discipline;
• monitoring experience and expertise in a CRO or pharmaceutical environment is an advantage;
• ability to work individually and in team;
• advanced in Lithuanian and English;
• motivated and enthusiastic individual.
• monitoring experience and expertise in a CRO or pharmaceutical environment is an advantage;
• ability to work individually and in team;
• advanced in Lithuanian and English;
• motivated and enthusiastic individual.
Company offers
• To work in a busy clinical research department providing essential monitoring support;
• to oversee the progress of a Clinical Trial;
• to work in an international company;
• business trips.
• to oversee the progress of a Clinical Trial;
• to work in an international company;
• business trips.