Elevate clinical trials with Syneos Health as a Bilingual Clinical Research Associate in Quebec. Engage in vital site management, regulatory compliance, and patient safety while working from home.
In this role, you will perform site qualifications, monitoring, and management while ensuring strict adherence to ICH-GCP and company protocols. Collaborate with diverse teams in a fully integrated biopharmaceutical setting, enhancing patient care through effective communication and diligent oversight. Your expertise in clinical operations and bilingual capabilities will contribute significantly to achieving project objectives.
Key Responsibilities:
- Conduct site qualification, initiation, and monitoring visits
- Ensure regulatory compliance with ICH and GCP guidelines
- Verify informed consent processes for patient confidentiality
- Assess patient safety and data integrity at sites
- Document all activities according to SOPs and clinical plans
Requirements:
- Bilingual in French and English
- Experience in clinical monitoring and site management
- Knowledge of ICH/GCP guidelines
- Strong analytical and communication skills
- Comfortable with remote work dynamics
Utilize your clinical expertise and bilingual skills to make a difference in patients' lives with Syneos Health.
Bilingual Clinical Research Associate - Quebec in Québec employer: 1001 Syneos Health, LLC
Syneos Health is an exceptional employer that fosters a collaborative and inclusive work culture, empowering employees to thrive in their careers while making a meaningful impact in the biopharmaceutical industry. With a strong commitment to professional development, competitive benefits including health coverage and a 401k match, and a focus on employee well-being, Syneos Health provides a dynamic environment where every team member can contribute to advancing healthcare solutions globally. Join us in shaping the future of patient care alongside a diverse team of experts dedicated to delivering innovative therapies.
