Directeur Commercial

About the role

We are seeking a Clinical Research Associate to join our team. The successful candidate will be responsible for monitoring clinical trials, ensuring compliance with regulatory requirements, and maintaining high-quality data standards.

Responsibilities

• Monitor clinical trial sites to ensure compliance with protocol, ICH-GCP, and applicable regulations
• Conduct site selection, initiation, monitoring, and close-out visits
• Verify the accuracy and completeness of case report forms against source documents
• Manage investigational product accountability and ensure proper storage and handling
• Identify and resolve site issues promptly, escalating as necessary
• Maintain effective communication with investigators, site staff, and internal teams
• Prepare and submit monitoring visit reports within required timelines
• Assist in the development and review of study documents and protocols

Qualifications

• Bachelor's degree in life sciences, pharmacy, nursing, or related field
• Minimum 2 years of clinical monitoring experience in a CRO or pharmaceutical company
• Thorough knowledge of ICH-GCP guidelines and applicable regulatory requirements
• Experience with electronic data capture systems and clinical trial management systems
• Strong organizational and time management skills
• Excellent written and verbal communication skills in English and French
• Ability to travel up to 40% as required

Skills

• Proficiency in Microsoft Office suite (Word, Excel, PowerPoint, Outlook)
• Strong attention to detail and problem-solving abilities
• Ability to work independently and collaboratively in a team environment
• Flexibility and adaptability to changing priorities