Clinical Research Associate

Job Description

As a Clinical Research Associate, you will manage the execution of clinical trials, monitor patient recruitment, and maintain quality data collection processes. Your work will directly contribute to medical advancements and improved patient care.

Responsibilities

• Manage all aspects of clinical trial operations.
• Liaise with healthcare professionals and site personnel to facilitate trial activities.
• Monitor and evaluate data quality and participant safety.
• Ensure the ethical treatment of participants throughout the study.
• Maintain accurate and timely documentation for all trial-related activities.
• Prepare for audits and inspections by regulatory bodies.
• Support the development of study protocols and procedural guidelines.
• Report findings and challenges to the Clinical Research Manager.

Requirements

Education

• Bachelor's degree in Nursing or Health Sciences
• Master's degree or equivalent experience preferred

Experience

• At least 3 years of experience in a clinical research environment

Technical Skills

• Data Analysis
• Patient Recruitment

Soft Skills

• Teamwork
• Attention to Detail

Certifications

• Clinical Research Coordinator (CRC)
• Project Management Certification

Languages

• English: Fluent

Advantageous

• Experience with Electronic Data Capture Systems: Knowledge of EDC systems for clinical data management is highly advantageous.
• Prior Experience in Patient-Engaged Research: Experience in studies involving patient engagement strategies would be beneficial.

Benefits

• Health, dental, and vision insurance
• Generous leave policy
• Support for continuing education and training
• Health and wellness programs

Company Culture

• Professional Growth: We provide ample opportunities for skill expansion and career development.
• Respect for Team Members: We respect and value the unique contributions of every employee.
• Empowerment: Our team members are empowered to take initiatives and lead projects.