Global Trial Director - Translational Research in Oncology (TRIO)

Translational Research in Oncology (TRIO) is a global clinical research organization dedicated to advancing translational cancer research in the clinical trial setting. Our passionate team is committed to providing cancer treatments of the future to the world of today.

 TRIO is seeking a dedicated and experienced Global Trial Director to join our Project Management team. As a Global Trial Director, you will play a critical role in overseeing and managing clinical trials, collaborating with cross-functional teams, and ensuring overall trial success.

Title: Global Trial Director - Translational Research in Oncology (TRIO) 

Company:                               Translational Research in Oncology (TRIO)

Business Address:                   Suite 1100 – 9925 109 St, Edmonton, AB, Canada T5K 2J8

Type of Employment:             Permanent, Full-Time (37.5 hours per week)

Language of Work:                 English

Job Duties:

–        Oversee and manage one or more clinical trials from start-up to completion.

–        Ensure overall trial delivery in terms of quality, timeliness, and cost.

–        Lead and provide operational support to cross-functional trial teams.

–        Develop and review trial timelines, management plans, and operational documents.

–        Allocate resources for trials and monitor trial metrics.

–        Assess risks and implement mitigation strategies.

–        Serve as the primary contact with sponsors for trial-related matters.

–        Mentor and manage project management team members.

–        Participate in the selection and evaluation of Third-Party Organizations (TPOs).

–        Ensure data quality and budget management for trials.

–        Participate in sponsor audits and bid defense meetings.

–        Collaborate with the VP of Project Management to define process changes.

–        Provide end‑to‑end leadership and accountability for one or more global clinical trials from start‑up through closeout, ensuring delivery to quality, timeline, and budget objectives.

–        Lead cross‑functional trial teams, providing operational expertise and ensuring achievement of trial milestones and deliverables.

–        Develop, review, and approve trial timelines, management plans, operational documentation, and training materials.

–        Ensure appropriate trial resourcing and proactively monitor performance metrics, risks, and mitigation plans.

–        Serve as the primary Sponsor contact, providing regular trial updates and delivering presentations, including at Investigator Meetings.

–        Mentor and manage Project Management team members; support PM hiring and talent development activities.

–        Select, oversee, and periodically evaluate Third Party Organizations (TPOs) involved in trial execution.

–        Ensure data quality and readiness for database lock in collaboration with internal departments.

–        Maintain financial oversight of assigned trials, including change orders, forecasting, and participation in financial review meetings.

–        Support sponsor audits, bid defense activities, and collaborate with leadership on process improvements and SOP updates.

Skills Requirements:

–        Education: Bachelor's degree (minimum), in a scientific field (Nurse, Scientist, Pharmacist, M.D.)

Experience:

–        At least 10 years of experience working on clinical trials.

–        5 years experience working on clinical trials in oncology

Key Competencies:

–        Fluent English

–        Strong leadership skills to effectively manage multi-disciplinary teams.

–        Excellent communication skills, both in written and orally.

–        Ability to build project plans incorporating all key elements of trial conduct.

–        Public presentation and sponsor interaction abilities

–        Excellent knowledge of ICH/GCP guidelines

–        Minimum intermediate proficiency in MS Office, including Word, Excel, MS Project, and PowerPoint

Wage:              150,000 – 200,000 annually

Benefits Package:       Health benefits, Dental plan, Disability benefits, Health care plan, Paramedical services coverage, Vision care benefits, Long term benefits, Life insurance, Registered Retirement Savings Plan (RRSP), 20 business vacation days. 10 personal days.

Business address / Location of Work: Suite 1100 – 9925 109 St, Edmonton, AB, Canada T5K 2J8

Criminal record check will be conducted as part of the hiring process. We invite qualified candidates who are passionate about oncology research and making a difference in the lives of patients to apply for this exciting opportunity. To apply please submit your resume to tatiana@lawpoint.ca