Lead clinical site activation from home in Quebec with IQVIA Biotech, applying regulatory strategy, study start-up, and project management expertise.

As an Associate Study Start-Up Manager, you will manage activation, maintenance, and regulatory activities for assigned studies or multi-protocol programs. The position covers scope, budgets, resources, timelines, and collaboration across Regulatory and Site Activation. You will support business development, study initiation, ongoing approvals, and clinical trial compliance.

Key Responsibilities:

- Oversee site activation and maintenance for assigned projects
- Develop management plans aligned with scope and strategy
- Determine regulatory strategies and submission expectations
- Maintain CTMS, databases, timelines,



and project plans
- Mentor colleagues and deliver presentations or training

Requirements:

- Bachelor's degree in life sciences or related field
- Seven years' relevant scientific or clinical experience
- International experience in a scientific or clinical workplace
- Knowledge of GCP, ICH, and applicable regulatory guidelines
- Strong negotiation, communication, leadership, and planning skills

Apply clinical trial oversight, regulatory expertise, and study start-up leadership to complex programs with IQVIA Biotech.

📌 Associate Clinical Study Start-Up Manager (Kirkland)
🏢 Lifelancer
📍 Kirkland