Clinical Research Associate

Job Description

As a Clinical Research Associate, you will play a crucial role in the planning, implementation, and monitoring of clinical trials. Your expertise will help ensure that our research projects are conducted ethically and efficiently, contributing to advances in patient care.

Responsibilities

• Conduct site visits to assess compliance with study protocols.
• Ensure timely collection, tracking, and reporting of trial data.
• Facilitate communication between sites and the central team.
• Actively contribute to the planning and execution of clinical research projects.
• Prepare and present trial updates to stakeholders.
• Support the development and refinement of clinical guidelines.

Requirements

Education

• Bachelor's degree in a relevant scientific discipline
• Advanced degree in Life Sciences or Public Health is an asset

Experience

• 3+ years of experience in clinical research, particularly in monitoring roles

Technical Skills

• Regulatory Compliance
• Patient Recruitment Strategies

Soft Skills

• Problem-Solving
• Team Collaboration

Certifications

• Certified Clinical Research Coordinator (CCRC)
• GCP Compliance Certification

Languages

• English: Fluent

Advantageous

• Familiarity with electronic data capture systems: Experience with systems like Medidata or Veeva Vault.
• Proven track record in site management: Demonstrated ability to effectively manage clinical trial sites.

Benefits

• Comprehensive healthcare coverage
• Flexible working arrangements
• Annual bonuses based on performance
• Employee wellness programs

Company Culture

• Innovation: We encourage innovative thinking and creative problem solving within our teams.
• Respect for Individuals: We celebrate diversity and treat all individuals with respect.
• Work-Life Balance: We support work-life balance for our employees' wellbeing.