Main Tasks

• Conduct monitoring activities for clinical investigations
• Liaise with investigational sites, from study initiation to close-out
• Generate monitoring plans and assist with completion of other clinical investigation documents
• Develop effective relationships with partners at investigational sites
• Ensure clinical investigations are conducted in accordance with the protocol, standard operating procedures, good clinical practice, and all applicable regulatory requirements

Requirements

• Education and/or experience equivalent to a Master’s degree in a scientific discipline
• Professional experience in clinical research, from either a medical device company or a CRO, is preferred
• Proficient language skills in English and German
• Good interpersonal, organizational and communication skills
• Willingness to travel (up to 30%)

 
 
Salary will be determined based on professional experience; the formal minimum salary according to Collective Bargaining Agreement is EUR 37,559.20.

We offer a challenging opportunity in a multinational work environment with English as our company language. We look forward to receiving your application at jobs.medel.com.