Pharmacovigilance Intern

As a Pharmacovigilance Intern at Miltenyi Biomedicine, you will play a crucial role in supporting the safety-related work of ongoing clinical trials. Your responsibilities will include assisting the Pharmacovigilance Department with various tasks, such as compiling and evaluating safety reports from clinical trials, and collaborating with other teams within the company and external stakeholders.

• Support the Pharmacovigilance Department with safety-related tasks
• Compile and evaluate safety reports from clinical trials
• Collaborate with other teams within the company and external stakeholders

• Completed 2nd state examination and in practical year of pharmacy studies
• First practical experience in pharmaceutical industry and clinical trials is advantageous
• Fast learner with ability to grasp new scientific concepts quickly
• Proficient in MS Office, especially Excel, PowerPoint, and Outlook
• Strong verbal and written communication in English

• Flexible working hours and mobile working
• Intercultural environment with diversity and flat hierarchies
• Freedom to contribute creatively and play an active role in shaping the company
• Individual further training in Miltenyi University
• 30 days of vacation, discounted ticket to Germany, e-bike leasing, and more

We look forward to receiving your application along with your salary expectations and availability.