Data Compliance Coordinator
Required skills
- ICH/GCP
- eCRF
- Investigator Site Files
- data integrity
- data protection
- quality control
- Microsoft Office
- medical terminology
Nice to have
- clinical research
- data management
- monitoring visit preparation
- bilingual skills
Role summary
Thermo Fisher Scientific is seeking a Corporate Compliance Associate II to support clinical trials. This role ensures data quality and regulatory compliance across research sites, coordinating operational compliance, maintaining documentation, and upholding data integrity standards. Responsibilities include eCRF data entry, query resolution, managing Investigator Site Files, and preparing for monitoring visits. The position requires strong attention to detail, time management, and proficiency in Microsoft Office and medical terminology, with a preference for experience in clinical research or data management.
Work Schedule
Standard (Mon-Fri)Environmental Conditions
OfficeJob Description
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.
DESCRIPTION:
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.
REQUIREMENTS:
• Relevant experience in clinical research, data management, or related field preferred
• Technical certification may be required for certain positions
• 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
• Bilingual skills may be required for specific positions
• Ability to work both independently and collaboratively in a team environment
• Experience with monitoring visit preparation and follow-up
• Knowledge of data protection regulations and compliance requirements
• Physical ability to be stationary for extended periods and perform computer work
