Job Overview

Join our global team as a Senior Clinical Research Associate (Level I), playing a key role in clinical monitoring and site management. You'll work with leading pharmaceutical companies and biotechs, ensuring that trials are conducted in compliance with regulations.

Key Responsibilities

• Monitor sites with a risk-based approach, ensuring compliance and data accuracy.
• Provide updates to the Clinical Team Manager and participate in investigator meetings.
• Ensure all essential documents are complete and conduct on-site file reviews.
• Facilitate communication between investigative sites and project teams.

Qualifications

A Bachelor's degree in life sciences or relevant qualifications is required, with 2+ years of clinical research monitoring experience preferred.

Skills

• Effective monitoring, critical thinking, and communication skills.
• Strong attention to detail and ability to manage risks.
• Proficiency in Microsoft Office and a good command of English.

Working Conditions

This role involves office work, site visits, and may require travel up to 60-80%. Personal protective equipment will be necessary due to potential exposure to biological fluids.