Job Title: Clinical Data Associate II
📍 Location: Bangalore, Karnataka, India
🆔 Job ID: R-01324178
🕒 Job Type: Full-time
🏢 Category: Clinical Research
🌐 Remote: Fully Remote
🗓 Work Schedule: Second Shift (1:00 PM – 10:00 PM IST)
⚠️ Environment: Adherence to Good Manufacturing Practices (GMP) safety standards
About Thermo Fisher Scientific
Thermo Fisher Scientific Inc. is the world leader in serving science, with annual revenue exceeding $40 billion. Our mission is to make the world healthier, cleaner, and safer. Through innovative technologies and services across industry-leading brands — Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon, and PPD — we empower our customers to solve complex challenges in life sciences, diagnostics, and therapeutics.
About Trialmed
This position is with Trialmed, the global site network and early-phase clinical research division of PPD, Thermo Fisher Scientific's clinical research business. Our Clinical Research team is committed to accelerating cures by providing top-tier scientific and clinical expertise to support the development of life-changing therapies.
Role Overview
As a Clinical Data Associate II (CDA II), you will support data management functions across early-phase clinical studies. You will play a critical role in data cleaning, validation, reconciliation, and query resolution—ensuring the quality and accuracy of clinical trial data. You’ll work cross-functionally in a fast-paced environment, applying your technical, analytical, and project coordination skills.
Key Responsibilities
📊 Data Management
Identify and resolve discrepancies in the clinical data management database
Generate, track, and manage data clarifications and queries
Review data listings for accuracy and consistency
Perform SAE and third-party vendor reconciliations
Support data listing reviews and CRF design implementation
🧪 Data Cleaning & Validation
Perform advanced data cleaning activities in compliance with GCPs and SOPs
Evaluate the safety and efficacy of investigational products/devices through data review
Analyze and resolve complex data validation issues
Produce status reports for CDM management and clients
🤝 Team Collaboration
Work cross-functionally and independently to resolve project issues
Provide input on project protocols and Data Validation Manual (DVM)
May act as a facilitator or team lead on assigned projects
Prepare and deliver internal and external communications with professionalism and tact
Qualifications
🎓 Education
Bachelor’s degree or equivalent formal academic qualification
Combination of education, training, and relevant experience may be considered
📈 Experience
Minimum 2+ years of experience in clinical data management or a related field
Skills & Competencies
💻 Technical Proficiency
Proficient with EDC systems, especially Medidata Rave and Veeva Vault
Familiar with eTMF and good documentation practices
Solid command of Microsoft Office tools and interactive software systems
🧠 Knowledge & Abilities
Understanding of clinical trial terminology, data validation processes, and protocols
Ability to manage confidential data with discretion
Skilled in analytical thinking, problem-solving, and time management
Familiarity with Generative AI tools is a plus
Adaptable, organized, and able to work independently or in teams
Strong interpersonal and customer focus skills
Excellent written and verbal English communication
Work Environment
Flexible work options: Office, remote, or hybrid
Second shift: 1:00 PM to 10:00 PM IST
Accessibility & Accommodations
We are committed to ensuring equal opportunity for individuals with disabilities. Reasonable accommodations will be provided throughout the application, interview, and employment process.
Equal Opportunity Statement
Thermo Fisher Scientific is an Equal Opportunity Employer. All qualified applicants will be considered without regard to race, color, religion, sex, gender identity or expression, sexual orientation, national origin, disability, age, veteran status, or any other protected status.
Why Join Us?
Work on high-impact clinical trials that drive life-saving treatments
Be part of a global leader in science and innovation
Thrive in a flexible, inclusive, and growth-oriented work environment
Join a mission-driven team focused on making a real difference in healthcare
🔗 Learn more at: www.thermofisher.com
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Siliguri |Illinois :
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