Clinical Research Associate

Vedi l’offerta su Go Lavoro: golavoro.it/annuncio-lavoro/8b19er

h3CRA - HOMEBASED ITALY /h3 pTFS HealthScience is a leading global mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire clinical development journey. Our expertise includes full service-capabilities, resourcing and Functional Service (FSP) solutions. /p h3Join Our Team as a Clinical Research Associate home-based in Italy /h3 h3About This Role /h3 pThe Clinical Research Associate (CRA) is part of Strategic Resourcing Solutions (SRS) within TFS Health Science and will function operationally as a member of a Project Team and is responsible for the initiation, on–site and/or remote monitoring, close out of study sites during study conduct, according to company policies, SOPs and GCP and ICH guidelines and other regulatory requirements. /p h3Key Responsibilities /h3 ul liMonitor on‑site and remotely clinical trials in accordance with TFS and/or sponsor Standard Operating Procedures GCP and ICH guidelines and applicable regulatory regulations. /li liPerform all required monitoring activities at the study sites to assess and ensure subjects safety, data integrity and quality. /li liVerify the protection of study participants by informed consent procedures and protocol requirements that follow appropriate regulations. /li liReview CRFs (electronic or paper) and subject source documentation for validity and accuracy. /li liVerify proper management and accountability of Investigational Product. /li liTimely reporting of actions taken during monitoring visits in Monitoring Visit Report including findings, corrective and preventive actions already taken and update applicable tracking systems, as required; escalated observed deficiencies and issues as appropriate.



/li liProviding site with the listing of issues identified during monitoring visit and action items which will need to be addressed in a timely manner. /li liTimely delivering site documents to eTMF or paper TMF; verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and ICH guidelines and local regulatory requirements. /li liParticipate in audit and/or inspection, its preparation and follow-up activities, as needed. /li liOrder, ship, and reconcile clinical investigative supplies for study sites, if applicable. /li liUpdate CTMS and all other required by projects systems with accurate site level information. /li /ul h3Qualifications /h3 ul liBachelor’s Degree, preferably in life science or nursing; or equivalent /li liAt least 3 years of experience monitoring clinical trials in Oncology /li liAble to work in a fast‑paced environment with changing priorities. /li liUnderstand basic medical terminology and science associated with the assigned drugs and therapeutic areas. Possess the understanding of Good Clinical Practice regulations, ICH guidelines. /li liAbility to work independently as well as in a team matrix organization. Strong written and verbal communication skills. Fluent in English. Excellent organizational skills. /li liTechnology savvy and good software and computer skills. /li liSoft skills: Self‑awareness, resolute, flexibility, proactivity, collaborative mindset, analytic approach, and attention to detail.



/li liAbility and willingness to travel up to 60‑80%, overnight and abroad if applicable. /li /ul h3What We Offer /h3 pWe provide a competitive compensation package, comprehensive benefits, and the opportunity for personal and professional growth in a rewarding environment. You’ll be joining a team that values collaboration, innovation, and making a difference in the lives of patients. /p pPermanent contract /p pSalary: gross/year (depending on the level of experience), in line with CCNL Terziario-Servizi (Level III), plus benefits (lunch vouchers, health insurance, pension, and car allowance where applicable) /p h3A Bit More About Us /h3 pOur journey began over 27 years ago in Sweden, in the city of Lund. As a full-service, global Contract Research Organization (CRO), we build solution‑driven teams working towards a healthier future. Bringing together over 800 professionals, TFS delivers tailored clinical research services in more than 40 countries with flexible clinical development and strategic resourcing solutions across key therapeutic areas including Dermatology, Neuroscience, Oncology, and Ophthalmology. /p pOur core values of Trust, Quality, Passion, Flexibility, and Sustainability are our guiding light serving as the framework for decision‑making at all levels of the organization. They assist us in attracting and retaining valuable talent who share our sentiments, resulting in high employee engagement and satisfaction. By aligning on these fundamental values, we cultivate a unified force, geared towards innovation and excellence. This collective effort propels us towards our shared goal and fosters a culture of mutual respect and collaboration. bTogether we make a difference. /b /p #J-18808-Ljbffr

Vedi l’offerta su Go Lavoro: golavoro.it/annuncio-lavoro/8b19er