Data Compliance Coordinator

About the role

As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world’s toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer.

Join our team at Thermo Fisher Scientific as a Corporate Compliance Associate II supporting clinical trials across our research sites. In this role, you'll ensure data quality and regulatory compliance while contributing to meaningful clinical research that improves health outcomes. You'll coordinate operational compliance activities across multiple studies, maintain critical documentation, and work closely with monitors and sponsor representatives to uphold the highest standards of data integrity. As part of our clinical research portfolio, you'll play an essential role in optimizing participant experiences in clinical trials and enabling life-changing therapies to reach those who need them.

Responsibilities

• Coordinate operational compliance activities across multiple clinical studies
• Maintain critical documentation and ensure data integrity
• Work closely with monitors and sponsor representatives to uphold regulatory standards
• Support the optimization of participant experiences in clinical trials
• Prepare for and follow up on monitoring visits

Requirements

• Relevant experience in clinical research, data management, or related field preferred
• Strong knowledge of ICH/GCP guidelines and regulatory requirements
• Proficient in electronic Case Report Form (eCRF) data entry and query resolution
• Experience maintaining Investigator Site Files (ISF) and study documentation
• Excellent attention to detail and quality control capabilities
• Strong time management skills with ability to handle multiple studies simultaneously
• Proficiency in Microsoft Office applications
• Ability to learn and apply medical terminology
• Strong verbal and written communication skills in English
• Ability to work both independently and collaboratively in a team environment
• Knowledge of data protection regulations and compliance requirements
• Physical ability to be stationary for extended periods and perform computer work
• Technical certification may be required for certain positions
• Bilingual skills may be required for specific positions