Clinical Research Associate

Under the general supervision of the Manager and Pathologist, the Pathologist's Assistant performs gross examining, describing, dissecting and sampling of Surgical Gross Specimens along with other supportive functions in the area. All primary functions are performed under the direction of a pathologist. Additionally you will be expected to engage in role-related teaching, professional development and research activities. • Bachelor’s degree in a health or science-related discipline required • Clinical Research Graduate Certificate preferred • Certification as a Clinical Research Professional (SoCRA or ACRP) an asset • 1-2 years previous related experience; Clinical research experience preferred • Knowledge of medical terminology required • Analytical thinking and problem solving skills • Excellent written and verbal communication skills • Knowledge of ICH-GCP guidelines, Health Canada Food and Drug Regulations, and Tri-Council Policy Statement 2 (TCPS-2) • Basic knowledge of clinical research principles, practices, and processes related to project management, study coordination, regulatory requirements, data collection and reporting • Highly proficient computer skills • Experience using electronic health records and data management software applications preferred • Ability to organize workload to meet deadlines and flexible when priorities change • Ability to push/pull carts with patient charts/case reports • Follows health and safety policies and procedures to ensure a safe workplace for self and others

The Pathologist's Assistant performs gross examination, description, and dissection of surgical specimens under the direction of a pathologist. Additionally, the role involves supporting clinical research activities, teaching, and professional development.

Candidates must hold a bachelor's degree in a health or science-related discipline and possess 1-2 years of relevant experience. Proficiency in medical terminology, clinical research principles, and regulatory guidelines such as ICH-GCP is required.

• written communicationSouhaitée
• Résolution de problèmesSouhaitée
• ReportingSouhaitée
• Gestion de projetSouhaitée

Relevées dans la description du poste. Confirmez les exigences importantes ci-dessus.

• Gross examining
• Dissecting
• Sampling
• Medical terminology
• Analytical thinking
• Problem solving
• Written communication
• Verbal communication
• ICH-GCP guidelines
• Project management
• Study coordination
• Regulatory requirements
• Data collection
• Reporting
• Electronic health records
• Data management software
• Analytical Thinking
• Ability To Meet Deadlines
• Research
• Teaching
• Medical Records
• Clinical Research
• Computer Literacy
• Data Collection
• Data Management
• Electronic Medical Record
• Pathology
• Good Clinical Practices (GCP)
• Problem Solving
• Project Management
• Medical Terminology
• Verbal Communication Skills
• Coordinating

• Healthcare
• Science & Research
• Administrative
• Clinical Research Associate
• Biologists, Botanists, Zoologists and Related Professionals
• Clinical Research Coordinators
• Natural Sciences Managers

Formation minimale

Diplôme professionnel

Expérience minimale

0+ ans

Postuler avant le

2 sept. 2026

Langue de l’offre

anglais

Heures de travail

40 heures par semaine