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.

Supports compliance to the clinical trial process. Helps ensure all study documentation and source data is captured accurately in eCRF, up to date and first time right. Assists with quality reviews and answers any eCRF queries for studies with low complexity in a timely manner. 

Day to Day

Maintains ISF and study trackers as delegated and supports the verification that ICFs are correctly completed. 

• Assists with data capturing activities on one or more studies.  
• Ensures accurate and timely entry of all data in the eCRF from the source notes and helps track the flow of the eCRFs and queries.    
• Assists with the verification that protocol visit windows are correct according to the protocol requirements and reports deviations/ Quality Incidents and participates in the investigation and resolution. 
• May assist monitors and sponsor representatives with query resolutions after monitoring visits. Escalates to management as needed.