Project Manager Clinical Operations (f/m/x)

locationsBerlinJenaOberkochenMünchenFull timeposted onPosted Todayjob requisition idJR_1034642This position can be held in Berlin, Munich, Jena or Oberkochen.Your role:Planning, implementation and management of international clinical studies with medical devices (primarily Intraocular Lenses, IOLs) according to applicable regulations and guidelines:Development of strategies and designs of clinical studies in cooperation with internal and external partners e.g., Contract Research Organizations (CROs)Creation of study-relevant documents that are necessary for regulatory approvals and their submission to responsible authorities and ethics committees.Ensuring the smooth running of the study projects by interacting with the study sites and acting as the central interface for the project stakeholders on a global scaleMonitoring of the study status and CRO activitiesReporting and presentations on the status as well as evaluation of the study resultsContribution to process development and evaluation of new regulations, guidelines, and standards for clinical studies.Your profile:College/university degree in Several years of experience in clinical affairs/clinical research project management in the medical device/ pharma industry or with CROsGood knowledge of relevant regulatory requirements for clinical studies for medical devices and experience in planning and conducting clinical studiesStrong analytical skills coupled with creativity and intuitionCommitment and creative drive as well as strong communication and organizational skills in an international environmentBusiness fluent English and German skills, both spoken and writtenWillingness to travel worldwideYour ZEISS Recruiting Team:Join us today. Inspire people tomorrow.Diversity is a part of ZEISS. We look forward to receiving your application regardless of gender, nationality, ethnic and social origin, religion, philosophy of life, disability, age, sexual orientation or identity.Apply now! It takes less than 10 minutes.