Clinical Research Associate

Job Description

As a Clinical Research Associate, you will play a crucial role in planning, implementing, and supervising clinical trials. Your expertise will help ensure that the trials meet all regulatory standards and that data collected is accurate and reliable.

Responsibilities

• Review site compliance with clinical trial protocols
• Conduct site assessments and provide feedback for improving practices
• Facilitate communication between sponsors, sites, and investigators
• Monitor inventory and ensure availability of study materials
• Support the clinical trials manager with project planning and execution

Requirements

Education

• Bachelor's degree in Nursing or Pharmacy is required

Experience

• 3+ years of experience in clinical trials or pharmaceutical industry

Technical Skills

• Data Analysis
• Project Management

Soft Skills

• Leadership
• Interpersonal Skills

Certifications

• Good Clinical Practice (GCP) Certification

Languages

• English: Fluent

Advantageous

• Knowledge of trial management software: Experience in using trial management software such as CTMS.
• Familiarity with patient recruitment strategies: Understanding of strategies to enhance patient recruitment.

Benefits

• Comprehensive health and dental insurance
• Retirement savings plan with matching contributions
• Opportunities for training and development
• Work-life balance support

Company Culture

• Commitment to Ethics: We uphold ethical standards in all our research initiatives.
• Continuous Improvement: We focus on continuous improvement and innovation in all our processes.
• Diversity and Inclusion: Our workplace celebrates diversity and is committed to inclusivity.