GERMANY - MUNICH |
As a qualified candidate, you should possess a science degree or equivalent, be fluent in German and English (knowledge of French is an advantage), minimum of 2 years experience in clinical research, have thorough knowledge of the AMG and ICH/GCP guidelines, and possess the communication skills necessary for working with a wide range of Investigators. Your goal will be to act as the primary contact of the project team with study site personnel, and to provide the Investigators with logistical and practical advice, training, assistance or support, thus ensuring the clinical trial is conducted in accordance with international regulatory and ethical guidelines for Good Clinical Practice. You are also expected to assist the Project Manager and the Senior CRA (SCRA) with the day-to-day running of international clinical studies. As an employer, Pharm-Olam International offers competitive remuneration packages, and excellent opportunities for career development in an open and pleasant working atmosphere. Please send your application, indicating the position applied for, as well as your salary expectations and earliest available start date, together with a comprehensive curriculum vitae to: hr-germany@pharm-olam.com |