Clinical Data Associate I (CDA I) – Remote, India
Company: Thermo Fisher Scientific (PPD Clinical Research Services)
Location: Remote – India
Job ID: R-01338259
Job Type: Full-time | Fully Remote
Category: Clinical Research / Clinical Data Management
Experience Required: 1–1.6 years
Work Schedule: Monday to Friday (Standard Business Hours)
Job Overview
Thermo Fisher Scientific, through its PPD® Clinical Research Services division, is hiring a Clinical Data Associate I (CDA I) to support global clinical trials in a fully remote capacity from India. This entry-level role is ideal for professionals with foundational experience in clinical data management who are looking to grow within a structured Functional Service Provider (FSP) model supporting a globally recognized biopharmaceutical sponsor.
The position focuses on clinical data cleaning, reconciliation, and query management while ensuring compliance with ICH-GCP, SOPs, and study protocols throughout the clinical trial lifecycle.
About the Organization
Thermo Fisher Scientific is a global leader in serving science, with annual revenue exceeding USD 44 billion and a workforce of over 90,000 employees worldwide. Through its PPD clinical research portfolio, the company has supported the top 50 pharmaceutical companies and more than 750 biotech organizations, delivering over 2,700 clinical trials across 100+ countries in the past five years.
Key Responsibilities
Perform entry-level clinical data cleaning and reconciliation activities with high accuracy.
Identify, review, resolve, and document data discrepancies in clinical databases.
Generate, track, and resolve data clarification forms (DCFs) and data queries.
Update clinical data management systems in accordance with study requirements.
Support CRF design and implementation using approved graphic design tools, as applicable.
Collaborate with cross-functional teams to ensure data integrity, inspection readiness, and timely issue resolution.
Adhere to ICH-GCP guidelines, global SOPs, work process documents (WPDs), and study protocols.
Maintain confidentiality of clinical trial data and sponsor proprietary information.
Education and Experience Requirements
Bachelor’s degree in Life Sciences, Pharmacy, Biotechnology, Clinical Research, or a related discipline.
Minimum 1 to 1.6 years of relevant experience in Clinical Data Management or Clinical Research.
Hands-on experience with RAVE and/or Veeva EDC platforms is mandatory.
Required Skills and Competencies
Strong understanding of clinical trial protocols and Data Validation Manuals.
High attention to detail with strong numerical and analytical skills.
Proficiency in interactive computer-based data management systems.
Good written and verbal communication skills with strong command of English.
Ability to work effectively under supervision while meeting quality and timeline expectations.
Strong problem-solving skills and sound judgment in decision-making.
Demonstrated flexibility, adaptability, and ability to work both independently and in team environments.
Commitment to maintaining high standards of data confidentiality and compliance.
Working Conditions
Fully remote role with standard office-based work requirements.
Occasional travel or site visits may be required based on project needs.
Work involves prolonged use of computer systems and office equipment.
Career Growth and Development
This role supports a client-dedicated FSP model for a globally established biopharmaceutical sponsor known for innovation in specialty medicines and vaccines. As part of this model, you will collaborate with global data science teams and contribute to high-visibility clinical programs.
Career progression opportunities include:
Senior Clinical Data Manager (Senior CDM)
Clinical Data Team Lead (CDTL)
Clinical Data Management Project Manager (CDM PM)
Transition opportunities into Data Standards or Clinical Programming
Continuous learning, mentorship, and structured development pathways are integral to this role.
Why Join This Role
Fully remote opportunity within India
Exposure to global, multi-phase clinical trials
Hands-on experience with modern CDM tools, EDC systems, and AI-enabled workflows
Opportunity to work with a top-tier global biopharmaceutical sponsor
Strong focus on quality, partnership, and long-term career growth
Equal Opportunity & Accessibility Statement
Thermo Fisher Scientific is an Equal Opportunity Employer. All qualified applicants will receive consideration without regard to any legally protected characteristic. Reasonable accommodations are available for individuals with disabilities throughout the recruitment and employment process.
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