Job Title: Clinical Data Associate I (CDA I)
Job ID: R-01338259
Location: Remote – India
Work Mode: Fully Remote
Job Type: Full-Time
Category: Clinical Research | Clinical Data Management
Experience Required: 1–1.6 Years
Thermo Fisher Scientific, through its PPD® Clinical Research Services, is a leading global Contract Research Organization (CRO) supporting the development of life-changing medicines. With experience across more than 2,700 clinical trials in over 100 countries and partnerships with the top pharmaceutical and biotechnology companies worldwide, Thermo Fisher Scientific is at the forefront of scientific and clinical innovation.
Thermo Fisher Scientific is hiring a Clinical Data Associate I (CDA I) to support global clinical studies through accurate and compliant clinical data management activities. This entry-level to early-career role focuses on clinical data cleaning, query management, and reconciliation while ensuring compliance with GCP, SOPs, and study protocols. The position offers exposure to global studies and strong long-term career growth within a structured Functional Service Provider (FSP) model.
Perform clinical data cleaning and reconciliation activities with high accuracy
Identify, investigate, resolve, and update data discrepancies within EDC systems
Generate, track, and resolve data queries and data clarification forms (DCFs)
Update and maintain clinical data management databases as required
Support CRF implementation and design activities using designated tools
Ensure data integrity, inspection readiness, and protocol compliance throughout the study lifecycle
Collaborate with cross-functional study teams to ensure timely issue resolution
1–1.6 years of hands-on experience in Clinical Data Management or Clinical Research
Practical experience working with RAVE and/or Veeva EDC systems
Understanding of GCP, clinical trial protocols, and Data Validation Manuals
Strong attention to detail with excellent analytical and problem-solving skills
Ability to work effectively under supervision while managing assigned tasks
Strong written and verbal communication skills with proficiency in English
Ability to handle confidential clinical and proprietary data responsibly
Bachelor’s degree or equivalent qualification in Life Sciences, Pharmacy, Clinical Research, or a related discipline
Standard working hours (Monday to Friday)
Office-based remote work environment
Occasional travel to clinical sites may be required
This role supports a dedicated FSP client, a globally recognized biopharmaceutical organization with a strong focus on specialty medicines, vaccines, and scientific innovation. As part of the FSP Data Management team, professionals gain:
Exposure to global, multi-phase clinical trials
Hands-on experience with modern CDM tools and AI-enabled workflows
Clear career progression pathways into Senior CDM, CDTL, CDM Project Management, or Data Standards and Programming roles
Continuous learning through structured training, mentorship, and stretch assignments
Work on international clinical trials across therapeutic areas
Gain end-to-end exposure from study setup to database lock
Build strong analytical, project management, and data quality expertise
Be part of a mission-driven organization advancing global healthcare
Thermo Fisher Scientific Inc. is the world leader in serving science, with annual revenues exceeding USD 44 billion. With more than 90,000 employees globally, the company enables customers to make the world healthier, cleaner, and safer through innovative technologies and pharmaceutical services.
Thermo Fisher Scientific is an Equal Opportunity Employer and is committed to fostering an inclusive and diverse workplace.
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