work. Your multifaceted tasks are to manage the clinical supplies situation, timelines and critical topics within assigned development projects of Boehringer Ingelheim provide the supply chain strategy for the IMP distribution to the project team represent the clinical trial support unit (CTSU) as subteam member for assigned projects at Medical and R&D subteam meetings, facilitate the supply chain process and report the clinical supplies situation assume responsibility for the evaluation and forecasting of bulk drug product and comparator needs of global phase I - IV projects ensure cross-functional collaboration and communication on project level to Medical and R&D subteams as well as to bulk manufacturing units and other units such as Global Sourcing, Legal and Logistics prepare regulatory documents for submission Your ideal qualification You hold a Diploma or Bachelor's Degree in Pharmaceutics, Biology or Life Sciences or gained an equivalent training in the pharmaceutical industry. In addition you possess at least 3 years of experience as a trial manager or project manager in a similar role, combined with thorough knowledge and understanding of the regulatory and GMP/GCP requirements in the pharmaceutical industry. Strong computer skills, especially in MS Office, go without s ...