Clinical Trial Manager II

This is a fully remote position, open to applicants in Canada.

📋 Description

• Accountable for the operational management and supervision of clinical investigative sites.

• Ensures that all clinical monitoring activities are executed accurately and in a timely manner.

• Identifies quality issues and trends associated with site performance.

• Acts as a primary point of contact for CRAs and Lead CRAs regarding assigned projects.

• Offers mentoring and guidance to CRAs and Lead CRAs.

• Prepares and delivers project-specific training sessions for CRAs.

• Develops annotated site visit reports along with monitoring tools.

• Organizes and leads meetings for CRAs.

⛳️ Requirements

• Bachelor's degree in a field pertinent to clinical research, nursing degree, or equivalent experience.

• Minimum of 8 years of experience in clinical research, including previous monitoring experience.

• At least 2 years of experience in a Lead CRA or Clinical Team Leader position within the biotechnology, pharmaceutical, or contract research organization (CRO) sectors.

• Solid understanding of ICH/GCP standards and relevant regulatory requirements.

• Proficient in the Microsoft Office suite (Word, Excel, PowerPoint).

• Capability to thrive in a fast-paced, dynamic environment while cultivating strong relationships with colleagues, sites, and sponsors.

• Exceptional leadership, organizational, time management, and multitasking abilities.

• Strong judgment and problem-solving capabilities.

• Willingness to travel occasionally (up to 10% of the time).

• Proficient in English (excellent oral and written skills), with French as an added advantage.

• Experience in a CRO and in dermatology is a plus.

🏝️ Benefits

• Flexible work schedule.

• Comprehensive benefits package (medical, dental, vision, vacation, personal days, virtual medical clinic, social activities).

• Continuous learning and professional development opportunities.