Clinical Research Associate - 12 Month Contract

You will be responsible for ensuring the successful execution of clinical trial activities at assigned sites while maintaining compliance with regulatory, protocol, and quality standards. This includes both operational monitoring and active collaboration with investigators and cross-functional teams.

• Conduct site qualification, initiation, monitoring (remote and on-site), and close-out visits in line with ICH-GCP, study protocols, and internal procedures
• Perform source data verification, source data review, and case report form reconciliation to ensure accuracy and completeness of clinical data
• Support regulatory and ethics submissions, including documentation preparation, tracking, and maintenance throughout the study lifecycle
• Train and support site staff on protocol requirements, study procedures, and Good Clinical Practice compliance
• Monitor patient safety reporting, including timely identification, documentation, and escalation of serious adverse events
• Manage investigational product accountability, study supplies, and essential document filing within the trial master file (eTMF)
• Ensure study sites remain inspection-ready and support audit and regulatory inspection activities as required
• Collaborate with data management and study teams to resolve queries, track progress, and ensure study timelines are met
• Provide ongoing updates on site performance, recruitment status, and quality metrics to study leadership

Requirements

You bring a strong foundation in clinical research and hands-on experience in site monitoring, with the ability to operate effectively in a regulated and fast-paced environment. You combine scientific understanding with strong organizational and communication skills.

• Bachelor’s degree in life sciences, pharmacy, nursing, or a related scientific discipline
• 2–5+ years of experience as a Clinical Research Associate or in clinical trial operations
• Strong knowledge of ICH-GCP guidelines, clinical monitoring practices, and regulatory requirements
• Experience performing SDV, SDR, and on-site/remote monitoring activities
• Familiarity with clinical trial systems such as CTMS and eTMF platforms
• Strong attention to detail with excellent documentation and reporting skills
• Ability to manage multiple studies and priorities while meeting strict timelines
• Strong interpersonal and communication skills for working with investigators and cross-functional teams
• Willingness to travel as required for site visits and monitoring activities

Benefits

• Competitive annual salary ranging from CAD 109,148 to CAD 143,257, depending on experience
• Contract-based role with access to structured benefits program
• Remote-friendly working arrangement with flexibility based on study needs
• Exposure to global clinical trials and cross-functional international teams
• Professional development opportunities within a leading clinical research environment
• Involvement in high-impact studies contributing to advancements in healthcare
• Supportive and collaborative team culture focused on quality and patient safety

We use an AI-powered matching process to ensure your application is reviewed quickly, objectively, and fairly against the role's core requirements. Our system identifies the top-fitting candidates, and this shortlist is then shared directly with the hiring company. The final decision and next steps (interviews, assessments) are managed by their internal team.

We appreciate your interest and wish you the best!

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