CRA I or higher

Job Overview

Thermo Fisher Scientific is seeking a Clinical Research Associate I (CRA I) or higher to join their team in Denmark. In this role, you will play a crucial part in supporting clinical trials, ensuring adherence to protocols, and contributing to the development of innovative scientific solutions for a healthier, cleaner, and safer world.

Company Overview

Thermo Fisher Scientific Inc. is the world leader in serving science, with annual revenue of approximately $40 billion. Our Mission is to enable our customers to make the world healthier, cleaner and safer. Whether our customers are accelerating life sciences research, solving complex analytical challenges, increasing productivity in their laboratories, improving patient health through diagnostics or the development and manufacture of life-changing therapies, we are here to support them. Our global team delivers an unrivaled combination of innovative technologies, purchasing convenience and pharmaceutical services through our industry-leading brands, including Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon and PPD.

Quick Details

• Salary Range: Market Competitive
• Job Type: Full-time
• Qualifications: Bachelor’s Degree
• Experience: 1 Year+

Key Responsibilities

• Assist in the initiation, monitoring, and close-out of clinical trials in accordance with ICH-GCP guidelines.
• Conduct source data verification and ensure accurate and complete documentation of trial data.
• Support site selection and qualification processes, including site visits.
• Collaborate effectively with study team members, investigators, and site staff to ensure smooth trial conduct.
• Maintain up-to-date knowledge of clinical trial regulations, company Standard Operating Procedures (SOPs), and relevant industry standards.
• Contribute to the overall quality and integrity of clinical trial data.

Requirements

• Bachelor’s degree in a life science, nursing, or a related scientific field.
• Minimum of 1 year of experience in clinical research or a related healthcare/pharmaceutical environment.
• Strong understanding of ICH-GCP guidelines and regulatory requirements.
• Excellent communication, interpersonal, and organizational skills.
• Ability to travel as required for site monitoring visits.
• Proficiency in English; knowledge of Danish is a plus.

Benefits

• Opportunity to work for a global leader in scientific research and innovation.
• Competitive salary and a comprehensive benefits package.
• Significant professional development and career growth opportunities within a diverse and global organization.
• Contribute to a vital mission of making the world healthier, cleaner, and safer.
• Work in a collaborative, supportive, and dynamic team environment.
• Access to cutting-edge technologies and scientific advancements.