Advance your career in clinical research with Alcanza as a Clinical Research Coordinator. This role focuses on the management of studies, patient interactions, and ensuring compliance with industry standards.

In this agile role, you'll play a key part in managing clinical trials across multiple therapeutic areas including neurology and dermatology. You will ensure effective execution of research protocols while prioritizing patient consent and maintaining accurate documentation throughout study phases. Engage with a collaborative team to enhance trial effectiveness and participant experiences.

Key Responsibilities:
• Obtain informed consent from study participants
• Follow up with patients during trial intervals
• Manage data entry and query responses in EDC




• Monitor and resolve study-related issues timely
• Ensure compliance with HIPAA and GCP guidelines

Requirements:
• Minimum 5 years in clinical research or relevant experience
• Proficiency in basic clinical procedures
• Strong organizational and communication abilities
• Self-motivated and capable of minimal supervision
• Must be willing to travel extensively

Utilize your clinical expertise and organizational skills to contribute to impactful research at Alcanza.
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📌 Join Alcanza as Clinical Research Coordinator (Ontario)
🏢 ActivMed Practices & Research
📍 Ontario