Clinical Research Associate

Job Description

As a Clinical Research Associate, you will play a vital role in managing clinical trials and ensuring compliance with regulatory standards. You will collaborate with cross-functional teams to monitor trial progress, collect data, and contribute to the successful execution of our research programs.

Responsibilities

• Monitor trial progress and report findings to senior management.
• Participate in the development and review of study protocols and documentation.
• Ensure compliance with Good Clinical Practice (GCP) and other relevant regulations.
• Facilitate communication between internal teams and external partners.
• Assist in financial tracking and management of trial budgets.
• Address any issues or challenges that arise during the trial process.

Requirements

Education

• Bachelor's degree in Health Sciences or related field
• Postgraduate qualification in Clinical Research is a plus

Experience

• 5+ years of experience in clinical trials

Technical Skills

• Clinical Data Analysis
• Project Management

Soft Skills

• Team Leadership
• Problem-Solving

Certifications

• ICH GCP Certification
• Certified Clinical Research Associate (CCRA)

Languages

• English: Fluent

Advantageous

• Prior Experience in Customer-facing Roles: Ability to manage client expectations and deliver updates effectively.
• Familiar with Electronic Data Capture (EDC) Systems: Experience with EDC systems for data collection and management.

Benefits

• Full medical, dental, and visual coverage
• Generous leave policies including paid time off
• Employee assistance programs
• Opportunities for further education and training

Company Culture

• Inclusivity: We are dedicated to creating an inclusive environment where all employees feel valued.
• Innovation: We encourage creativity and new ideas to enhance our research capabilities.
• Community Engagement: We actively engage in community health initiatives and outreach programs.