Project Manager, Early Phase and Translational Research / Gestionnaire de projet, phase précoce

The Project Manager, Early Phase and Translational Research (Gestionnaire de projet, phase précoce) at Indero in Canada oversees the full lifecycle of early‑phase clinical research projects, from initiation through closure, ensuring compliance, budget control, and high‑quality site management.

Key Responsibilities

• Lead the planning, execution, monitoring, and closure of early‑phase clinical trials.
• Coordinate with investigative sites, CROs, and internal teams to ensure timely delivery of monitoring activities.
• Maintain project budgets, scope, and timelines while managing risks and issues.
• Prepare project documentation, status reports, and regulatory submissions.
• Ensure all trial activities comply with GCP, ICH, and local regulatory requirements.
• Facilitate communication between sponsors, sites, and cross‑functional departments.

Qualifications & Skills

• Bachelor’s degree in life sciences, pharmacy, nursing, or related field; Master’s preferred.
• Minimum 3 years of project management experience in early‑phase or translational clinical research.
• Strong knowledge of clinical trial processes, monitoring, and site management.
• Excellent organizational, analytical, and problem‑solving abilities.
• Proficient in project management tools (MS Project, Smartsheet) and clinical trial software (e.g., Medidata, Veeva).
• Fluent in English; French language skills are an advantage.

Why Join Indero?

Indero offers a collaborative environment where innovative research meets rigorous project execution. You will contribute to groundbreaking therapies while advancing your career in a supportive, globally‑connected team.

Frequently Asked Questions

What type of clinical projects will I manage?

You will oversee early‑phase and translational research trials, handling everything from site initiation to study close‑out.

Do I need French language skills for this role?

Fluency in English is required; French is a plus but not mandatory.

What experience is required?

At least three years of project management experience in early‑phase clinical research, with a strong understanding of GCP and site monitoring.