THE CLEAREST PATH TO CAREER FULFILLMENT STARTS WITH PAREXEL. At PAREXEL, we believe that the power to work independently and intelligently should be yours every day. Your ability to understand our clients' needs and achieve quality results is critical to our reputation as one of the best clinical research organizations (CROs) in the world. On your PAREXEL journey, we support you with leading-edge technology, the highest caliber team members, and managers who know your strengths. If you're looking for flexibility and work-life balance, we're here to listen and help you move forward with your individual career path. Bring your talent to PAREXEL and surround yourself with colleagues who share the same dedication and passion-to deliver life-saving treatments to patients worldwide. PAREXEL Poland is looking for Clinical Research Associates (various levels). The role is full time and can be office based in Warsaw or home based (limitations apply) PAREXEL provides monitors with world class technology, training resources, and limited protocol load. You will also be rewarded for your hard work through our CRA bonus incentive program and career advancement opportunities. Key Accountabilities:- Perform all clinical monitoring/site management activities for assigned projects in accordance with PAREXEL's standard operating procedures. - Act as PAREXEL's direct contact with assigned clinical sites, and use judgment to assess and ensure overall integrity of study implementation, as well as adherence to study protocol.- Conduct qualification visits (QV), site initiation visits (SIV) and monitoring visits (MV) at assigned clinical sites.- Good knowledge of applicable clinical research regulatory requirements; i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.- Function as a mentor and role model for other CRA team members.- Manage clinical monitoring activities, including: Arranging on-site visits and logisticsEstablishment of a site recruitment plan in collaboration with site staff during QVMonitoring completeness and quality of Regulatory Documentation Performing site documentation verificationData collection and drug accountability in accordance with ICH GCP guidelineMonitoring patient safety on-site and addressing any violations in a timely manner Key Qualifications:- Previous documented monitoring experience in clinical research.- Excellent communication skills.- Educated to degree level (biological science, pharmacy or other health related discipline).- Strong working knowledge of EDC systems and IVRS.- Experience of CTMS preferred.- Competent in written and oral English and Polish. Our Offer: We offer you a fascinating and diversified insight into PAREXEL and an exciting journey through the world of clinical research. You can expect to work with a successful, highly-qualified and dynamic team as you develop your individual scientific profile. You can also look forward to a flexible working environment and a pleasant atmosphere.