Elevate clinical research at Worldwide Clinical Trials as a bilingual Clinical Research Associate. Leverage your expertise in Oncology and manage diverse clinical study activities across Canada.In this senior position, you will oversee research activities at various sites while supporting regulatory compliance and safety reporting. With extensive interaction in the Oncology field, your role will encompass study initiation, budget negotiation, and site training. You will collaborate with a committed team and receive prospects for qualified growth toward Clinical Trial Manager roles.Key Responsibilities:
Manage clinical research activities at participating sites
Conduct study initiation visits (SIVs) effectively




Ensure compliance with informed consent and safety reporting
Negotiate contracts and budgets with sites
Train sites on data collection and reporting protocolsRequirements:
5+ years as a Clinical Research Associate
4-year degree or Nursing Degree required
Oncology experience is mandatory
Fluent in English and French, both written and spoken
Willingness to travel regionally for site visitsDrive impactful clinical research and make a difference in patients' lives with Worldwide Clinical Trials.#J-18808-Ljbffr

📌 Bilingual Clinical Research Associate Canada Quebec City
🏢 Worldwide Clinical Trials Holdings
📍 Quebec City