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.
Position Summary:
Join our Clinical Research team as a Corporate Compliance Associate III, where you'll contribute to ensuring the quality and integrity of clinical trials. In this position, you'll coordinate operational compliance activities across multiple studies, managing data and documentation to support medical research. You'll work with clinical research tools, ensuring accurate data entry, maintaining regulatory compliance, and contributing to the successful delivery of clinical studies that impact patient lives.
Requirements:
• Strong knowledge of ICH‑GCP guidelines and regulatory requirements.
• Expertise in clinical trial documentation and source data verification.
• Proficiency in CRF completion and query management.
• Experience with quality control processes and CAPA procedures.
• Strong understanding of protocol compliance and deviation reporting.
• Ability to prepare and manage regulatory documentation.
• Advanced proficiency in Microsoft Office applications.
• Exceptional attention to detail and accuracy.
• Strong organizational and time‑management skills.
• Ability to manage multiple studies and priorities simultaneously.
• Excellent verbal and written communication skills.
• Fluency in English required.
• Knowledge of data protection regulations and privacy requirements.
• Experience with clinical trial management systems.
Responsibilities:
• Expertise in clinical trial documentation and source data verification.
• Proficiency in CRF completion and query management.
• Experience with quality control processes and CAPA procedures.
• Strong understanding of protocol compliance and deviation reporting.
• Ability to prepare and manage regulatory documentation.
Experience:
• Minimum 1 years of experience in clinical research data management and compliance.
• Experience with clinical trial management systems.
• Experience with quality control processes and CAPA procedures.
Education:
• Preferred fields of study: Life Sciences, Healthcare, or related field.
• Clinical Research Associate (CRA) certification or equivalent preferred.
Physical Requirements / Work Environment :
• Onsite work in an office and laboratory environment.