Job Title: Clinical Data Associate I (CDA I)
Location: Remote – India
Job Type: Full-time
Category: Clinical Research / Data Management
Job ID: R-01338259
Company Overview:
Thermo Fisher Scientific is a global leader in serving science, with over 90,000 employees worldwide and annual revenue exceeding $44 billion. Our mission is to enable customers to make the world healthier, cleaner, and safer by supporting life sciences research, analytical challenges, patient diagnostics, and laboratory efficiency. Our Clinical Research team powers PPD® clinical research services, delivering high-quality study execution for top pharmaceutical and biotech companies globally.
Role Summary:
The Clinical Data Associate I will perform entry-level clinical data management tasks, ensuring high-quality data cleaning, reconciliation, and query resolution. This role contributes to data integrity and inspection-readiness throughout the study lifecycle while working collaboratively with cross-functional teams in a fully remote setup.
Key Responsibilities:
Identify, resolve, and update data discrepancies in clinical databases.
Generate, track, and resolve data clarifications and queries.
Perform initial CRF design in designated graphic design packages, as needed.
Maintain adherence to GCP, SOPs/WPDs, study protocols, and client expectations.
Ensure confidentiality and security of clinical and proprietary data.
Collaborate with cross-functional study teams to support timely issue resolution and data accuracy.
Education & Experience Requirements:
Bachelor’s degree or equivalent in Life Sciences, Pharmacy, or related fields.
1–1.6 years of experience in clinical data management or relevant roles.
Hands-on experience with RAVE / Veeva EDC platforms.
Required Knowledge & Skills:
Strong attention to detail and numerical accuracy.
Proficient in interactive computer programs and clinical data management systems.
Excellent written and verbal communication skills in English.
Analytical and problem-solving abilities.
Ability to work independently with direct supervision and in team environments.
Familiarity with project protocols, Data Validation Manuals, and clinical trial processes.
Flexibility, adaptability, and good judgment in decision-making.
Working Environment:
Primarily office or remote-based work with exposure to standard office equipment.
Occasional travel to site locations may be required.
Career Growth & Opportunities:
As part of our FSP (Functional Service Provider) model, you will support a globally recognized biopharmaceutical client in specialty medicines, vaccines, and scientific innovation. This role offers:
Exposure to international clinical studies across multiple phases and therapeutic areas.
End-to-end involvement in study delivery, from set-up to close-out.
Hands-on experience with modern CDM, including AI-enabled workflows.
Career advancement paths in Clinical Data Management (Senior CDM, CDTL, CDM PM) or Data Standards/Programming.
Mentorship, tailored learning pathways, and opportunities to work on high-visibility, complex initiatives.
Why Join Thermo Fisher Scientific:
Contribute to life-changing medicines delivered worldwide.
Gain global exposure and work with leading CROs, vendors, and international teams.
Develop analytical, project management, and clinical trial technology skills in a dynamic environment.
Work for a global leader committed to innovation, quality, and scientific excellence.
Equal Employment Opportunity Statement:
Thermo Fisher Scientific is an equal opportunity employer. All employment decisions are made without regard to race, religion, color, age, sex, sexual orientation, gender identity, disability status, or any other legally protected status.
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