Clinical Research Associate in România

PRA Health Sciences is a Clinical Research Organisation experiencing exceptional growth globally. The people we employ are key to this growth.We believe that our people are the future of the industry. We provide a culture in which our employees can enjoy personal satisfaction, professional achievement and have the ability to strategically map out long-term career plans. If you're ready to be a part of something inspiring join us and Discover Your PRA.We are currently seeking a Clinical Research Associate to join our Clinical Operations team based in Romania, Bucharest.Working fully embedded within one of our pharmaceutical clients, with the support of PRA right behind you, you’ll be at the heart of our client’s innovation.As Clinical Research Associate, you will be dedicated to one of our global pharmaceutical clients; a science-based company with one of the most exciting product pipelines in the industry. This global pharmaceutical client develops breakthrough innovative medicines to improve and extend people’s lives in oncology, general medicine and eye care. Working in this way, you will have the opportunity to build your career in a rewarding customer-focused environment that supports creativity, collaboration and performance.The Clinical Research Associate is ultimately responsible for the successful management of investigator sites and monitoring activities for assigned clinical studies throughout the trial lifecycle. Key responsibilities include:Full ownership of investigator sites for assigned studies, with responsibility for the successful management of the site right through to close-out, in accordance with the clinical monitoring plan.Developing effective relationships with investigator site staff to ensure that key clinical metrics are met.Ensuring integrity of clinical data through an ability to sufficiently maintain site tracking records and working diligently to relevant guidelines.You are:Dedicated, collaborative and inspire others.Here at PRA we want our employees to succeed and ensure that they are set up for this success through constant training, development and support. To enable success in this position you will have: * Prior experience of working in investigator site management, including conducting monitoring visits, from either a pharmaceutical company or a CRO environment. * A working knowledge of ICH-GCP guidelines and local and international regulatory requirements is essential. * You will be educated to degree level, have equivalent experience or be a licensed healthcare professional.Your health, your family, your career, your money — the things that matter to you, matter to us. The benefits of PRA just get better and better.*PRA Health Sciences is an Equal Opportunity Employer. We welcome and encourage diversity in the workplace.*