Working Student (m/f/d) Clinical Affairs

at  Olympus Europa SE Co KG OEKG

Your responsibilities

• As a Working Student (m/f/d), you support the Clinical Project Managers in the planning, execution, and close-out of clinical studies sponsored by Olympus.
• You perform systematic literature research and acquisition on specific clinical topics using research strategies on medical databases. You analyze and evaluate the identified literature according to defined criteria.
• Researching the regulatory requirements for clinical studies in different countries is part of your Tasks.
• You upload and organize contracts in the Olympus contract database.
• You also support the clinical data management.
• Other administrative and organizational tasks are part of your responsibilities.

Your qualification

• You are an enrolled student of Medicine, Biology, Pharmacology or another natural science course (at least 3rd semester)
• Ideally, you have basic knowledge of medicine and/or the medical industry
• Practical experience in conducting literature research is an advantage
• A confident handling of MS Office is a matter of course for you
• You have a very good command of written and spoken English
• You are characterized by analytical skills, initiative and team orientation

Your benefits

• 17 EUR per hour
• Proportionate vacation entitlement
• Interesting and diverse tasks in an international working environment
• Excellent mentoring structure with regular feedback
• Up to 60% remote work is possible

We look forward to receiving your complete application including cover letter, CV and references! Please apply via our website by clicking on “Apply now”. Applications via mail cannot be taken into consideration.

• As a Working Student (m/f/d), you support the Clinical Project Managers in the planning, execution, and close-out of clinical studies sponsored by Olympus.
• You perform systematic literature research and acquisition on specific clinical topics using research strategies on medical databases. You analyze and evaluate the identified literature according to defined criteria.
• Researching the regulatory requirements for clinical studies in different countries is part of your Tasks.
• You upload and organize contracts in the Olympus contract database.
• You also support the clinical data management.
• Other administrative and organizational tasks are part of your responsibilities