Thermo Fisher Scientific looking for Clin Data Associate

Thermo Fisher Scientific Inc is the world leader in serving science. Our mission is to enable our customers to make the world healthier, cleaner and safer. With revenues of 13 billion USD, we have approximately 39,000 employees and serve customers within pharmaceutical and biotech companies, hospitals and clinical diagnostic labs, universities, research institutions and government agencies, as well as in environmental and process control industries. We create value for our key stakeholders through three premier brands, Thermo Scientific, Fisher Scientific and Unity™ Lab Services, which offer a unique combination of innovative technologies, convenient purchasing options and a single solution for laboratory operations management.

Post : Clin Data Assoc I

Job Description
Role Overview
This role is responsible for entry-level clinical data cleaning and reconciliation activities performed with high accuracy and in accordance with GCP, SOPs/WPDs, and study protocols. You will collaborate with cross-functional study teams to ensure data integrity, timely issue resolution, and inspection-readiness of study data throughout the study lifecycle.
• Identifies, resolves, and updates data discrepancies. Makes changes to the data management database as required.
• Generates, tracks and resolves data clarifications and queries.
• May implement CRF design in identified graphic design package.

Candidate Profile
• Bachelor's degree or equivalent and relevant formal academic
• Previous experience (Min 1 to 1.6 Years) that provides the knowledge, skills, and abilities to perform the job
• Should have experience in RAVE / Veeva EDC

Knowledge, Skills and Abilities
• Applies knowledge and skills in a highly organized fashion while adhering to regulatory guidelines, global SOPs and client expectations
• Strong attention to detail and skill with numbers
• Ability to use interactive computer programs
• Good written and verbal communication skills and a strong command of English language and grammar
• Good analytical /problem-solving skills
• Ability to work productively with direct supervision
• Ability to maintain a high degree of confidentiality with clinical data and client's proprietary data
• Proven flexibility and adaptability
• Ability to work in a team environment and independently as needed
• Must demonstrate good judgment in making decisions
• Understands project protocol and Data Validation Manual

Additional Information
Experience : Min 1 to 1.6 Years
Qualification : Bachelor's degree
Location : Remote, India
Industry Type : Pharma/ Healthcare/ Clinical research
Functional Area : Clinical Research
End Date : 30th January 2026