Job Title: Clinical Data Associate I
Location: Remote, India
Job Type: Full-time
Category: Clinical Data Management / Clinical Research
Thermo Fisher Scientific is a global leader in serving science, committed to enabling customers to make the world healthier, cleaner, and safer. With over 90,000 colleagues worldwide and annual revenue exceeding $44 billion, we deliver innovative technologies and pharmaceutical services through our trusted brands, including Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, and Patheon.
Our clinical research services, powered through PPD®, support top pharmaceutical and biotech companies across 2,700 clinical trials in over 100 countries, ensuring life-changing therapies reach patients safely and efficiently.
As a Clinical Data Associate I (CDA I), you will play a key role in maintaining high-quality clinical data through entry-level data cleaning, reconciliation, and validation activities. Working closely with cross-functional study teams, you will ensure data accuracy, regulatory compliance, and inspection readiness throughout the study lifecycle. This is an excellent opportunity for professionals aiming to build a career in Clinical Data Management (CDM) with exposure to global clinical trials and advanced data technologies.
Identify, resolve, and update data discrepancies in clinical trial databases.
Generate, track, and resolve data queries in compliance with study protocols.
Assist in CRF design implementation and data validation tasks.
Collaborate with cross-functional study teams to maintain data integrity and ensure timely issue resolution.
Maintain accurate project documentation and adhere to regulatory guidelines, SOPs, and client expectations.
Apply organizational, analytical, and problem-solving skills to ensure high-quality data management practices.
Uphold confidentiality of clinical data and proprietary client information.
Bachelor’s degree in Life Sciences, Pharmacy, Medicine, or a related field.
Experience: 1–1.6 years in Clinical Data Management or related roles.
Hands-on experience with RAVE / Veeva EDC platforms.
Strong command of English (written and verbal) with excellent communication skills.
Attention to detail, analytical mindset, and ability to follow structured processes.
Ability to work independently and in a team environment while maintaining confidentiality.
Familiarity with project protocols, Data Validation Manuals, and global CDM best practices.
Adaptability, flexibility, and willingness to learn advanced data management processes.
Experience contributing to AI-enabled workflows or modern clinical data technologies.
This position is part of Thermo Fisher’s FSP Data Management team, supporting a globally recognized biopharmaceutical client. Career paths include:
Clinical Data Management Track: Progression to Senior CDM, Clinical Data Team Lead (CDTL), or CDM Project Manager.
Data Standards & Programming: Transition opportunities based on skill, impact, and business needs.
Global Exposure: Work on international clinical trials across multiple phases and therapeutic areas.
End-to-End Ownership: Engage in all stages of study delivery, from set-up to close-out.
Skill Development: Enhance project management, data analysis, risk management, and AI-enabled CDM skills.
Impact: Contribute to life-changing medicines and innovative healthcare solutions worldwide.
Apply Now: Submit your resume/CV through Thermo Fisher Scientific’s careers portal or via our FSP program application.
Thermo Fisher Scientific is an Equal Opportunity Employer and values diversity in the workplace.
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