Project Manager

📋 Description

• Support the initiation, planning, execution, monitoring, control, and closure of assigned clinical
• Serve, when assigned, as a primary point of contact for sponsors, vendors, internal teams, and
• Coordinate tasks, resources, and deadlines across departments to support timely study delivery and
• Work with project coordinators, site start-up teams, regulatory and clinical resources, and vendor
• Monitor project milestones and site activation progress, escalate risks or delays to senior project
• Support resource planning, project status reporting, study tracker reconciliation, change control

🎯 Requirements

• Bachelor's degree in a relevant field related to clinical research or a comparable discipline.
• At least three years of experience in a similar role, including clinical study management
• At least two years of experience coordinating clinical trial management activities.
• Strong knowledge of GCP and International Council for Harmonisation (ICH) standards, as well as
• Proficiency in Microsoft Office applications and the ability to prepare accurate project
• Excellent written and spoken English; French language skills are an advantage.

🎁 Benefits

• Permanent, full-time position.
• Flexible working schedule to support work-life balance.
• Vacation allowance.
• Home-based working arrangement, subject to role and location eligibility.
• Ongoing learning, training, and professional development opportunities.
• A stimulating, science-driven environment with collaborative colleagues.