CDA I
Thermo Fisher Scientific · Bengaluru
Other
Thermo Fisher Scientific is hiring a CDA I in Bengaluru, Karnataka. Posted 17 October 2026. Apply directly on Thermo Fisher Scientific's own careers site — no account needed.
Work Schedule
Standard (Mon-Fri)Environmental Conditions
OfficeJob Description
Join Us as a Clinical Data Associate I – Make an Impact at the Forefront of InnovationWe have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700 clinical trials across 100+ countries in the last 5 years.
As part of our global team, you’ll have the opportunity to perform entry-level aspects of the data cleaning process with a high level of accuracy and in accordance with GCPs and SOPs/WPDs to assess the safety and efficacy of investigational products and/or medical devices.
What You’ll Do:
• 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.
Education and Experience Requirements:
• High / Secondary school diploma or equivalent and relevant formal academic / vocational qualification
• Technical positions may require a certificate
• Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to at least 4 years).
In some cases an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.
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
Working Conditions and Environment:
• Work is performed in an office or clinical environment with exposure to electrical office equipment.
• Occasional drives to site locations. Potential Occasional travel required.
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