Clinical Project Manager - Montréal, Canada (F / M)

Keyrus Biopharma SA; Montreal; On-site; CAD 80,000 - 110,000; Full time

Job summary

A growing biotech company is seeking a Clinical Project Manager in Montreal to lead clinical trials. The ideal candidate will have a Master's degree and 5-8 years of experience in clinical operations, especially in immuno-oncology. This full-time role offers opportunities for professional growth and an inclusive work environment.

Benefits

Opportunities for professional growth

Personalized support and career development

Continuous learning through internal training academy

Recognized as #TopEmployer2025

Qualifications

• 5-8 years of experience in clinical operations.
• Experience in managing Phase I / II clinical trials in immuno-oncology.
• Familiar with clinical study management tools.

Responsibilities

• Manage and coordinate various aspects of clinical trials.
• Develop comprehensive plans for clinical trials.
• Ensure compliance with regulatory standards and timelines.

Skills

Clinical operations experience

Knowledge of ICH GCP

Adaptability

Organizational skills

Project management

Education

Master's degree in a scientific discipline

Tools

eCRF databases

Job description

Join us to apply for the Clinical Project Manager - Montréal, Canada (F / M) role at ALSINOVA CRO.

What We Will Accomplish Together

Alsinova is seeking an experienced expert in clinical research and healthcare management to serve as a Clinical Project Manager. Join our growing team in Canada and enhance your career potential.

Your Mission (should You Decide To Accept It)

Responsibilities include managing and coordinating various aspects of clinical trials.

Strategic Planning

Your daily activities will be :

• Develop comprehensive plans for initiating, executing, and completing clinical trials, aligning them with project goals and timelines.
• Contribute to creating and refining study protocols, outlining methodology, objectives, informed consent forms (ICF), electronic case report forms (eCRF), and other study-related documents.
• Identify and manage risks associated with clinical trials and make recommendations.
• Ensure compliance with regulatory standards, timelines, and budgets.
• Supervise clinical research associates and documentation specialists, and train team members on project operations.
• Manage vendors to ensure patient safety, contract adherence, data integrity, and financial engagement. Act as the primary contact for vendors.
• Prepare and review documents related to clinical projects (contracts, vendor budgets, reports). Facilitate communication between research teams, sponsors, and regulatory authorities.
• Participate in data analysis, summaries, and reporting for regulatory requirements.
• Hold at least a Master's degree in a scientific discipline (biology, biomedical sciences, pharmacy) or equivalent.
• Have 5-8 years of experience in clinical operations, including field follow-up, CRO, and supplier management.
• Previous experience with Phase I / II clinical trials in immuno-oncology.
• Knowledge of ICH GCP and relevant legislation.
• Familiar with clinical study management tools and systems (eCRF databases).
• Ability to work independently, adapt to changing situations, and maintain high-quality work.
• Enthusiastic about joining a fast-growing biotech company.
• Other qualities: organized, pragmatic, flexible, persistent, open-minded, results-oriented.

Our Benefits

• Opportunities for professional growth and diverse projects.
• Personalized support and career development.
• Continuous learning through our internal training academy.
• Inclusive and friendly work environment, recognized as #TopEmployer2025.

Seniority level

• Mid-Senior level

Employment type

• Full-time

Job function

• Project Management and Information Technology
• Health and Human Services

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