CTM/Clinical Trial Manager

System One - 2 emplois

Burlington, ON

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Publié il y a 30 jours Expire bientôt !

Détails de l'emploi :

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Temps plein

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Assurance vie

Job Title: Clinical Trial Manager Location: Hybrid, Metro Toronto (Burlington) - 50% per month onsite Type: 12 months contract Pay: 50 to 60 per hour CAD Join a dynamic clinical research team as a Clinical Trial Budgets & Contracts Specialist, where you'll play a key role in managing multi-million-dollar clinical trial budgets and negotiating study contracts that help bring innovative therapies to patients. This hybrid opportunity is ideal for professionals with experience in clinical research, budgeting, and contract management who enjoy collaborating with cross-functional teams in a fast-paced environment. Accountable for the trial activities for responsible R/ OPU, including but not limited to:
Ensure the trial is conducted in compliance with GCPICH, local/global regulations, applicable SOPs and according to the trial protocol by overseeing CRO and internal team activities.
Creation, management and review of the R/OPU trial budget to ensure appropriate level of financial oversight and planning accuracy. Timely budget updates based on trial changes.
Appropriate trial-specific training of R/OPU internal and external partners is performed in line with Trial Training Plan.
Oversees outsourcing of vendor services in the R/OPU in accordance to operating models and governance.
Maintains oversight during clinical trial conduct including adherence to GCP and all global and local regulatory requirements; compliance with SOPs and continuous risk monitoring/mitigation. In collaboration with other functions, ensures budget oversight, including support of regular clinical quality monitoring, and safety reporting.
Monitor progress of patient recruitment endpoints and proactively update and action contingencies throughout trial conduct.
Minimum Education/Degree Requirements* Degree /education: Requires a university degree (e.g. Masters degree or comparable degree) with several years relevant experience in required area. Major focus: Biomedical Life Sciences System One, and its subsidiaries including Joulé, ALTA IT Services, and Mountain Ltd., are leaders in delivering outsourced services and workforce solutions across North America. We help clients get work done more efficiently and economically, without compromising quality. System One not only serves as a valued partner for our clients, but we offer eligible employees health and welfare benefits coverage options including medical, dental, vision, spending accounts, life insurance, voluntary plans, as well as participation in a 401(k) plan. System One is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, age, national origin, disability, family care or medical leave status, genetic information, veteran status, marital status, or any other characteristic protected by applicable federal, state, or local law. Ref: #568-Clinical

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Foire aux questions

What is the location and work setup for this Clinical Trial Manager role?

This is a hybrid role based in Metro Toronto (Burlington), with 50% onsite per month.

What is the contract duration and how much does this job pay per hour?

The position is a 12-month contract with pay ranging from $50.00–$60.00 per hour CAD.

What are the main responsibilities of this Clinical Trial Budgets & Contracts Specialist role?

You will manage the R/OPU trial budget, oversee vendor outsourcing, ensure regulatory and SOP compliance, provide trial-specific training, and monitor recruitment progress and safety reporting.

What qualifications are required for this Clinical Trial Manager position?

A university degree (e.g., Masters) with several years of relevant experience in biomedical life sciences, budgeting, and contract management is required.

What regulatory and quality standards will this role require adherence to?

The role requires compliance with GCPICH, local/global regulations, applicable SOPs, and continuous risk monitoring/mitigation during the trial.

Who will I collaborate with in this role?

You will collaborate with cross-functional teams and external partners to oversee CRO activities and training per the Trial Training Plan.

Who is the employer for this job and is it a permanent position?

The job is offered by System One as a full-time contract role for 12 months, not a permanent position.