Clinical Research Associate

2 settimane fa


WorkFromHome, Italia Whatjobs A tempo pieno

Join to apply for the Senior CRA role at Thermo Fisher Scientific 1 day ago Be among the first 25 applicants Join to apply for the Senior CRA role at Thermo Fisher Scientific Work Schedule Other Environmental Conditions Office At PPD, part of Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100 countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on – now and in the future. This is a great opportunity for experienced Senior CRA's currently working within the life science sector for pharmaceutical companies, biotech companies or CRO's to work with a world-leading CRO across multiple sponsors, various protocols and therapy areas. These roles can be performed remotely for CRA's based close to our clinical 'hubs' : Milan, Bologna, Florence, Rome and Naples. Travel requirement will be national across Italy. Essential Functions : Monitors investigator sites with a risk-based monitoring approach : applies root cause analysis (RCA), critical thinking and problem-solving skills to identify site processes failure and corrective / preventive actions to bring the site into compliance and decrease risks. Ensures data accuracy through SDR, SDV and CRF review as applicable through on-site and remote monitoring activities. Assess investigational product through physical inventory and records review. Documents observations in reports and letters according to timelines using approved business writing standards. Escalates observed deficiencies and issues to clinical management expeditiously and follows all issues through to resolution. May need to maintain regular contact between monitoring visits with investigative sites to confirm that the protocol is being followed, that previously identified issues are being resolved and that the data is being recorded in a timely manner. Participates in the investigator #J-18808-Ljbffr



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