IHR PROFIL:

• Natural science/scientific background (FH, university)
• At least 3 years experience in pharmaceutical industry
• Experienced in medical writing of clinical and regulatory documents
• Experienced in clinical trial development
• Good knowledge of international and national/regional guidelines and regulatory topics
• Being able to work independently, manage multiple projects
• Fluency in English and German (written and spoken)
  For this position, the salary applies from € 3.200,- to € 3.900,- gross per month or € 44.800,- to € 54.600,- gross per year. An overpayment in line with the market, depending on qualifications and professional experience, is offered.
  We are looking for ambitious, highly qualified and motivated employees, who are team-oriented and willing to show self-initiative. We recruit employees who share GL Pharma´s philosophy of innovation and growth and are willing to develop on both a personal and an educational level.
  Bitte bewerben Sie sich aus datenschutzrechtlichen Gründen ausschließlich über unsere Homepage. Nach dem Abschicken Ihrer Bewerbung erhalten Sie eine Empfangsbestätigung

Please refer the Job description for details