Job Description

Syreon’s Clinical Project Management Division is looking for a Clinical Research Coordinator (CRC) to join our multi-disciplinary unit in the ongoing support of cutting-edge research programs. This full-time role is an opportunity to collaborate with a dynamic team of researchers in maintaining the highest standards in the conduct of research activities. The Research Coordinator will work cohesively with all internal departments and external clients such as site investigators, site coordinators, Sponsor, monitors, 3rd party vendors, Scientific Advisory Committee, and Research Ethics Boards to facilitate a wide range of project activities.

The successful applicant will work closely with our Project Management, IT, Data Management, Operations, and QA Divisions to maintain the highest standards to conduct our research programs. Strong organizational and personal effectiveness skills, including ability to seek information, result-orientation, self-management, and time management are essential.

SYREON is a full-service Clinical Research Organization. We combine elite biomedical sciences, advanced technologies, and global clinical trial networks to speed the evaluation of new drugs, diagnostics and medical devices and guide their safe, effective, and cost-efficient clinical use. We conduct international clinical trials and health economics and outcomes research across a broad range of chronic and rare diseases.

In this role, you will:

• Review study protocols, informed consent templates, and prepare Central Ethics Boards submissions and resubmissions as required
• Develop and/or review study documents (e.g., Project Plans, Risk Management Plan, Risk Logs, Gantt Charts, etc.)
• Plan, coordinate, and attend Investigator’s Meetings
• Set-up, collect, maintain, and quality check all Trial Master Files, include eTMFs
• Set-up and distribute Site Investigator Binders
• Recruit, train, and provide ongoing support to participating sites, Sponsors, monitors, and third-party vendors
• Management of Investigational Product
• Develop and execute Site Recruitment strategies
• Develop and update content on study websites as well as manage user access requirements
• Support site payment administration
• Prepare agenda and minutes for study meetings (internal, with sponsor and with external parties)

To be successful in this role, you likely have:

• One to three years industry experience within a CRO/Pharmaceutical/Biotech company preferred
• BSc in life sciences or medically related field, preferably OR three years of industry experience preferably in a CRO/Pharmaceutical/Biotech environment
• Excellent Clinical Research/Clinical Trials knowledge
• Excellent knowledge and understanding of ICH/GCP/FDA and Health Canada Regulations
• Excellent competency in Microsoft Office
• Excellent ability to work independently and effectively in project teams, take ownership and responsibility for actions

Benefits

• 3 weeks of paid vacation
• Paid sick days
• Extended health & dental plan fully paid by employer
• Health care spending account
• Opportunities for professional growth and career advancement

Ready to join our team?

If you like to be challenged and prefer working with a team committed to excellence, then we would like to hear from you. Apply with your cover letter and resume at

Find out more:

For more information about Syreon, please visit our website:

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