Clinical Trial Coordinator – FSP

Job Overview

Thermo Fisher Scientific is seeking a Clinical Trial Coordinator – FSP to join their team in Finland. In this crucial role, you will be instrumental in coordinating clinical trials, ensuring smooth operations, and contributing to advancements in life sciences research. You will support the execution of studies that help make the world healthier, cleaner, and safer.

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. For more information, please visit www.thermofisher.com.

Quick Details

• Salary Range: Market Competitive
• Job Type: Full-time
• Qualifications: None / Open to all applicants
• Experience: 2 Year+

Key Responsibilities

• Coordinate and support all phases of clinical trial activities according to protocol and regulations.
• Manage essential trial documentation, ensuring accuracy and compliance with GCP and SOPs.
• Facilitate communication and collaboration between study sites, sponsors, and internal teams.
• Assist in the preparation and submission of regulatory documents and ethics committee applications.
• Monitor study timelines and progress, identifying and resolving potential operational issues.
• Ensure the integrity and quality of clinical trial data through diligent oversight and verification.

Requirements

• Proven experience in clinical research or a related healthcare field.
• Strong understanding of clinical trial processes, GCP guidelines, and regulatory requirements.
• Excellent organizational skills and meticulous attention to detail.
• Effective communication and interpersonal skills for interacting with diverse stakeholders.
• Proficiency in Microsoft Office Suite and clinical trial management systems.
• Ability to work independently and collaboratively in a fast-paced environment.

Benefits

• Opportunity to contribute to cutting-edge scientific research and patient health.
• Work within a global leader serving science with a strong mission.
• Competitive salary and a comprehensive benefits package.
• Access to continuous professional development and career advancement opportunities.
• Collaborative and innovative work culture focused on making a global impact.
• Exposure to industry-leading technologies and brands in life sciences.