Clinical Data Associate I

Roles & Responsibilities

• Lead advanced data review and cleaning activities to ensure data integrity, timeliness, and inspection readiness
• Manage complex queries and perform SAE and third-party data reconciliations
• Review data listings and validation outputs for accuracy
• Contribute to CRF design and database updates
• Generate, track, and resolve data clarifications and queries
• Produce project-specific status reports for CDM management and clients
• Perform data management activities, including Serious Adverse Event (SAE) and third-party vendor reconciliations
• Support and collaborate with cross-functional teams to resolve issues and risks
• Safeguard the accuracy and analysis-ready datasets for safety and efficacy assessments

Qualification

• Bachelor's degree or equivalent and relevant formal academic training

Experience

• 1.6 to 3 years of experience in clinical data management or relevant field
• Experience in RAVE / Veeva EDC

Skills

• Strong attention to detail with proficiency in numbers and interactive computer programs
• Excellent organizational, analytical, and problem-solving skills
• Strong written and verbal communication skills in English
• Ability to work independently and collaboratively in a team environment
• Knowledge of medical/clinical trial terminology
• Understanding of project protocol and Data Validation Manual
• Ability to maintain confidentiality with clinical data

About The Company

Thermo Fisher Scientific is a global leader in serving science, with annual revenue exceeding $44 billion. The company supports life sciences research, accelerates diagnostics, and offers laboratory services to make the world healthier, cleaner, and safer.