Clinical Research Associate 1

Job Overview

Thermo Fisher Scientific is seeking a Clinical Research Associate 1 to join their team in Finland. In this role, you will be responsible for supporting the execution of clinical trials, ensuring compliance with protocols and regulatory requirements, and contributing to the advancement of scientific research.

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: 2 Year+

Key Responsibilities

• Assist in the execution of clinical trials according to protocol, standard operating procedures, and regulatory guidelines.
• Monitor clinical sites for compliance with study protocols, SOPs, and Good Clinical Practice (GCP).
• Ensure accurate and timely collection of clinical data and source documentation.
• Support site selection, initiation, monitoring, and close-out activities.
• Prepare and submit study-related documents to regulatory authorities as required.
• Maintain effective communication with investigators, site staff, and internal teams.

Requirements

• Bachelor’s degree in a life science, health science, or related scientific field.
• Minimum of 2 years of experience in clinical research or a related healthcare environment.
• Solid understanding of Good Clinical Practice (GCP) and regulatory requirements (e.g., FDA, EMA).
• Strong organizational skills and attention to detail.
• Excellent verbal and written communication skills in English; Finnish language skills are a plus.
• Ability to travel both domestically and internationally as needed for monitoring visits.

Benefits

• Competitive compensation package and comprehensive benefits.
• Opportunities for professional growth and career advancement within a global industry leader.
• Work with cutting-edge technologies and contribute to life-changing therapies.
• Engage in a collaborative, innovative, and supportive international work environment.
• Contribution to a mission that makes the world healthier, cleaner, and safer.
• Access to global learning and development programs.