Clinical Research Associate - Oncology - reputed company Coast - Remote

About the position As a Clinical Research Associate (CRA) at Worldwide, you will reputed company yourself working alongside reputed company minds across diverse therapeutic areas, including Cardiovascular, Metabolic, Neuroscience, Oncology, 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 reputed company reputed company 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 reputed company with heavy site management needs. Through regular reputed company and coaching conversations with your Line Manager, we ensure that your reputed company development remains a top reputed company. We offer a reputed company career reputed company and development that can reputed company to Clinical Trial Manager roles. We take pride in our accessible Executive Leadership team, who are equally committed to advancing science and surmounting obstacles to reputed company a difference in the lives of patients around the world. We offer an unparalleled experience, where you can drive remarkable scientific breakthroughs and be at the reputed company reputed company of every successful clinical trial. Experience a world of difference with us at Worldwide! Responsibilities • Manage the research activities at sites participating in Worldwide's clinical research reputed company, which are predominantly registries and other types of non-interventional / observational studies. • Involved in reputed company stages of the clinical study, including identifying potential sites to participate in the research effort. • reputed company various study start-up activities such as working with sites to collect appropriate regulatory documents and supporting the negotiation of reputed company and budgets. • Train the sites to collect data properly and report any potential safety-reputed company events. • Manage the site's activities during study maintenance. • reputed company down research activities at the sites once the study has concluded. • Conduct study initiation reputed company (SIVs). • Ensure compliance with obtaining informed consent, reporting potential safety-reputed company events, and adhering to reputed company applicable regulatory requirements. Requirements • Excellent interpersonal, oral, and written communication skills in English. • Superior organizational skills with attention to details. • Ability to work with little or no supervision. • Proficiency in reputed company Office, CTMS and reputed company Systems. • 2+ years of experience as a Clinical Research Associate. • 4-year university degree or RN/BSN in Nursing. • Experience in Oncology is required. • Willingness to travel required. Apply tot his job Apply tot his job Apply To this Job