Clinical Trial Assistant - S

3K Consulting Inc; Uxbridge; On-site; CAD 60,000 - 80,000; Full time

Job summary

A healthcare consulting firm located in Ontario is seeking a talented professional to manage clinical trials. The role requires strong computer skills in EXCEL and MS Word, and proficiency in project planning and tracking. Candidates should ideally possess a bachelor’s degree in life science or relevant experience in clinical trials. Excellent communication and organizational skills are key to success in this role, contributing to high-quality clinical development projects.

Qualifications

• Familiar with clinical trial and drug development processes.
• Ability to learn new planning and tracking systems quickly.
• Proficiency in resource management and clinical trial management.

Responsibilities

• Track projects in clinical planning and tracking systems.
• Ensure accuracy and data integrity in reports.
• Work with cross-functional teams to meet timelines.

Skills

Strong computer skills (EXCEL, MS Word)

Communication skills

Organizational skills

Attention to detail

Ability to work independently

Knowledge of project reporting tools

Customer focused

Education

Bachelor degree or equivalent in life science/healthcare

3 years clinical trials experience if no degree

Job description

Responsibilities

• Familiar with clinical trial and drug development process.
• Ability to work in clinical planning and tracking systems, and to learn new systems readily.
• Strong computer skills (EXCEL, MS Word) required. Knowledge of project reporting tools, preferred.
• Demonstrated proficiency in applying basic principles and procedures for resource management, project planning/tracking, and clinical trial management.
• Strong understanding of interdependencies of various clinical databases and implications on business process when databases are changed.
• Great attention to accuracy and detail. Comfortable with data in table/report format.
• Good communication, organizational, and tracking skills. Customer focused.
• Ability to work with cross-functional teams, meet timelines and work independently.
• Thorough understanding of clinical trial conduct and regulation.

Education

Bachelor degree or equivalent education/degree in life science/healthcare is preferred OR If no degree, 3 years clinical Trials experience required, such as in clinical development, drug development or project management with experiencing work in clinical planning and tracking systems.

Additional Information

All your information will be kept confidential according to EEO guidelines.