We’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 protected. It is built by those who take pioneering, creative approaches and implement them with quality and excellence.At 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) you will work alongside brilliant minds across therapeutic areas including Cardiovascular, Metabolic, Neuroscience, Oncology, and Rare Diseases.What You Will DoResponsible for managing the research activities at sites participating in Worldwide’s clinical research projectsTypically involved in all stages of the clinical study, including identifying potential sites to participate in the research effort, performing various study start-up activities such as working with sites to collect appropriate regulatory documents and supporting the negotiation of contracts and budgets, training the sites to collect data properly and report any potential safety-related events, managing the site's activities during study maintenance,



and closing down research activities at the sites once the study has concludedConduct study initiation visits (SIVs)While most of the site management efforts will be performed remotely, you will be required to ensure compliance with obtaining informed consent, reporting potential safety-related events, and adhering to all applicable regulatory requirementsWhat You Will Bring To The RoleExcellent interpersonal, oral, and written communication skills in EnglishSuperior organizational skills with attention to detailAbility to work with little or no supervisionProficiency in Microsoft Office, CTMS, and EDC SystemsYour Experience5+ years of experience as a Clinical Research Associate4-year university degree OR Nursing DegreeExperience in Oncology is requiredFluent in written and verbal English and French is requiredCandidates must reside in CanadaWillingness to travel regionally requiredWorldwide is an equal opportunity employer that is committed to enabling professionals from all backgrounds and experiences to succeed. We 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.#J-18808-Ljbffr

📌 Senior Clinical Research Associate (Bilingual) - Oncology - Canada (Remote)
🏢 Worldwide Clinical Trials
📍 Quebec City