Contract Specialist (Clinical Trials) - Legal Services - Regular Full-Time 2026-18114
Sunnybrook Health Sciences Centre —Toronto, ON
- Temps plein
- Sens de l'organisation
- Contrats
- Affaires
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Contract Specialist (Clinical Trials) - Legal Services - Regular Full-Time 2026-18114
Sunnybrook Health Sciences Centre —Toronto, ON
Diploma or degree in law, business, health administration or equivalent. 2–5 years of relevant experience in clinical research contracting or legal document…
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Contract Specialist (Clinical Trials) - Legal Services - Regular Full-Time 2026-18114

Sunnybrook Health Sciences Centre -
Toronto, ON

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Détails du poste

Temps plein

Profil recherché

Gestion des contrats
Droit
Amélioration des processus
Gestion des archives
Rédaction juridique
Sens de l'organisation
Contrats
Essais cliniques
Gestion des documents
Affaires
Compétences en communication
Coordination d'équipe

Description complète du poste

Sunnybrook Health Sciences Centre – Toronto, ON

Sunnybrook Health Sciences Centre is advancing its position as a global leader in clinical research through a strategic initiative focused on reducing study activation timelines and improving the experience for sponsors and investigators.

We are seeking a Clinical Trials Contracts Specialist to join our Legal Services – Clinical Trials team. This role is central to executing fast-track clinical trial agreements, helping accelerate study start-up while maintaining high standards of quality and compliance.

About the Role

You will be part of a team of four professionals supporting clinical research, reporting to the Senior Legal Counsel (Research).

Your primary focus will be fast-track clinical trials—agreements that rely on pre-approved templates or existing master agreements and meet defined criteria for streamlined execution. You will also support broader clinical trial work as capacity allows.

Key Responsibilities

Draft, review, and process fast-track clinical trial agreements using standard templates and master agreements
Coordinate efficient agreement execution with internal stakeholders and external partners
Ensure agreements meet Sunnybrook fast-track criteria and quality standards
Support Sunnybrook’s strategic initiative through template use, workflow improvements, and cycle time reduction, including liaising with Sunnybrook’s Centre for Clinical Trial Support
Engage with industry sponsors and CROs to encourage use of master agreements
Assist with non-fast-track clinical trial agreements as workload permits
Maintain accurate records and track agreement status and metrics

Qualifications

Diploma or degree in law, business, health administration or equivalent
2–5 years of relevant experience in clinical research contracting or legal document management
Familiarity with clinical trial agreements or legal contracting processes is an asset

What You Bring

Proactive, solutions-focused approach
Strong attention to detail and organizational skills
Ability to manage a high volume of agreements efficiently
Process-oriented mindset focused on speed and consistency
Excellent communication and coordination skills
Comfort working in a structured, template-driven environment

Why Join Sunnybrook

Contribute directly to accelerating access to innovative clinical trials
Be part of a high-impact institutional initiative
Work with a collaborative, mission-driven team
Develop specialized expertise in clinical trial contracting

Apply

Interested candidates are encouraged to apply with a resume and cover letter through Sunnybrook’s careers portal.

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