Drug Safety Intern - Czech Republic

As an Intern in our Safety data management team you will:

Support Pharmacovigilance (PV) department units as needed
Perform project and department related activities and delegated activities as assigned
Work in close collaboration with other colleagues

What will be your key responsibilities:

Assistance with PV related tasks
Administrative work at the department – may include, but is not limited to:
Editing, scanning, printing, and filing/archiving of the documents according to good documentation practice and Arriello quality system;
Revision, formatting, editing of functional project documents – templates, tables, reports, manuals, and plans;
Technical support of PV Department in pharmacovigilance-oriented tasks, e.g., Global Literature Monitoring – reviewing medical journals for the presence of safety information, Case Processing
Adherence to the company’s processes and systems
Organize and maintain project files and keep databases updated
Education in Pharmacovigilance processes

Ongoing/newly completed studies in pharmaceutical sciences or related fields – medicine, pharmacy, life sciences
Fluent verbal and written English
Excellent team player, able to work as part of a team
Organizational and time-management skills, able to prioritize work and adhere to deadlines
Excellent communication skills
Maintains a positive, results-oriented work environment