ph3Who we are /h3pWe're a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world's most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence. We are Worldwide Clinical Trials, and we are a global team of over 3,500+ experts, bright thinkers, dreamers and doers and, together, we are changing the way the world experiences CROs - in the best possible way. Our mission is to work with passion and purpose every day to improve lives and we are looking for others who value this same pursuit. /ph3Why Worldwide /h3pWe believe everyone plays an important role in making a world of difference for patients and their caregivers. From our hands-on, accessible leaders, to our cohesive and supportive teams, we are committed to enabling professionals from all backgrounds and experiences to succeed. We prioritize cultivating a diverse and inclusive environment that continues to promote collaboration and creativity. We are proud to be a workplace where people thrive by being themselves and are inspired to do their best work every day. Join us! /ph3What Clinical Operations does at Worldwide /h3pAt Worldwide Clinical Trials, we invite you to embark on a rewarding journey within Clinical Operations, where your contributions will leave a profound impact on the lives of patients. As a Clinical Research Associate (CRA) at Worldwide, you will find yourself working alongside brilliant minds across diverse therapeutic areas, including Neuroscience, Oncology, Cardiovascular, Metabolic and Rare Diseases. Collaboration with top-tier colleagues from various backgrounds and specialties is not just encouraged; it's ingrained in our culture.



Our commitment to advancing clinical research is nurtured within a supportive and team-oriented environment. In a CRA role, you'll receive extensive support through regulatory submissions, TMF management, and in-house CRAs for projects with heavy site management needs. /ph3What you will do /h3ulliResponsible for site qualification, initiation, interim monitoring, site management, and study close-out visits. /liliProvide mentoring and guidance to less experienced CRAs and site staff when needed. /liliDocument site visit findings via written reports. /liliAssess, monitor, and train study site staff on protocol adherence as required. /liliReview study subject safety information and informed consent. /liliConduct source document verification for compliance, patient safety, and veracity of data. /liliReview CRFs using paper or electronic data capture systems and assist sites with data query resolution. /liliProvide applicable updates for site related documentation for filing in the Trial Master File (TMF). /liliEnsure site compliance with IP receipt, accountability and return or destruction. /liliConduct accompanied site visits for assessment or training of other CRAs as requested and appropriate. /li /ulh3What you will bring to the role /h3ulliExcellent interpersonal, oral, and written communication skills in English /liliSuperior organizational skills with attention to details /liliAbility to work with little or no supervision /liliProficiency in Microsoft Office,



CTMS and EDC Systems /li /ulh3Your experience /h3ulli2+ years of experience as a Clinical Research Associate /lili4-year university degree or RN/BSN in Nursing /liliExperience in Oncology and Hematology is required /liliWillingness to travel required /li /ulpWe love knowing that someone is going to have a better life because of the work we do. /ppFor more information on Worldwide, visit or connect with us on LinkedIn. /ppWorldwide is an equal opportunity employer that is committed to enabling professionals from all backgrounds and experiences to succeed and, to that end, we prioritize attracting diverse talent and cultivating an inclusive environment that encourages collaboration and creativity. /ppWe know that when our employees feel appreciated and included, they can be more creative, innovative, and successful. /ppWe're on a mission to hire the very best and are committed to creating exceptional employee experiences where everyone is respected and has access to equal opportunity. /ppWe provide equal employment opportunities to all employees and applicants regardless of race, color, ethnicity, ancestry, religion, national origin, gender, sex, gender identity or expression, sexual orientation, age, citizenship, marital or parental status, disability, military status, or other class protected by applicable law. /ppThis is who we are. /ppWe're a team of clinicians, scientists, and researchers who want to make healthcare better. /ppWe were founded on an unwavering commitment to authentic, personalized attention. /ppAnd today, as CROs consolidate and the industry changes rapidly, that personalized attention is more important than ever. /ppWe all came to this industry for different reasons, from different walks of life. If you ask any one of us why we're here, you'll get a different answer. /ppAnd that's what makes us special. /p /p #J-18808-Ljbffr

📌 Clinical Research Associate - Oncology, Hematology - Italy (Italia)
🏢 Worldwide
📍 Italia