Study Coordinator – CRO

Role Overview

The Study Coordinator supervises the planning for clinical studies, supervises and/or performs all technical functions necessary to generate data in compliance with protocols, SOPs and GCP.

What You Will Do

Responsibilities include but are not limited to: ensuring study protocols, preparing study-specific staff schedules, coordinating with departments, supervising technical functions, and ensuring subject safety.

Why It Might Be a Fit

The Study Coordinator will be part of an inclusive, adaptable, and forward-thinking organization, with opportunities for advancement and career progression.

Requirements

• Minimum B.Sc. degree
• 1 year Phase I clinic experience or 2 years related experience within a Phase I clinical center
• Clinical Research Coordinator designation as per ACRP guidelines
• Excellent understanding of Phase I study protocols and conduct
• Understanding of the value and necessity of training and SOP’s relating to study conduct GCP training
• Excellent computer skills
• Excellent communication skills
• Ability to communicate clearly and effectively with direct reports and other clinical staff
• Excellent interpersonal skills
• Ability to work both independently and as a team member
• Exceptional organizational skills

Benefits

• Competitive compensation plan
• A benefit plan that is fully paid for by PMRI, including healthcare, dentalcare, vision care, LTD, Life Insurance, AD&D, along with a Health Spending and Wellness Spending Accounts and a voluntary RRSP Contribution Plan
• Opportunities for advancement and career progression
• A generous Employee Milestones Awards Program
• Corporate Discounts Program
• Friendly atmosphere, culture of learning

Tagged as: Compensation Design