Clinical Data Associate I (CDA I) – Remote, India
Location: Remote, India
Job ID: R-01338259
Job Type: Full-Time
Category: Clinical Research / Clinical Data Management
Work Mode: Fully Remote
About the Role
Thermo Fisher Scientific is seeking a Clinical Data Associate I (CDA I) to join our global Clinical Research team. This entry-level role is ideal for professionals with 1–1.6 years of experience in clinical data management, eager to grow within a leading global contract research organization (CRO).
As a CDA I, you will play a key role in ensuring data integrity, accuracy, and inspection readiness across international clinical trials. You will collaborate with cross-functional teams to clean, reconcile, and validate clinical trial data in accordance with GCP guidelines, study protocols, SOPs, and WPDs.
Key Responsibilities
Identify, resolve, and update clinical data discrepancies with precision and timeliness.
Generate, track, and resolve data clarifications and queries.
Support CRF design implementation in designated graphic design tools, if required.
Ensure data quality and integrity for accurate downstream analysis.
Collaborate with global CDM teams to maintain study timelines and inspection readiness.
Education & Experience Requirements
Bachelor’s degree or equivalent in Life Sciences or a related field.
1–1.6 years of experience in clinical data management, preferably using RAVE or Veeva EDC.
Understanding of clinical trial protocols and data validation manuals.
Skills & Competencies
Strong attention to detail and numerical accuracy.
Proficiency in interactive data management systems and computer applications.
Good written and verbal communication skills in English.
Analytical and problem-solving skills to identify and resolve data issues.
Ability to maintain confidentiality of clinical and proprietary data.
Flexibility to work independently or collaboratively within a team environment.
Ability to follow SOPs and adhere to global regulatory standards.
Working Conditions
Primarily remote work with occasional travel to site locations as required.
Office or clinical environment exposure with standard office equipment.
Career Growth & Learning Opportunities
Join our FSP Data Management team supporting a globally recognized biopharmaceutical client. This role offers:
Global exposure: Work across international clinical trials spanning multiple therapeutic areas and phases.
End-to-end project ownership: Contribute to data management from study setup to close-out.
Career progression: Opportunity to advance along the Clinical Data Management track (e.g., Senior CDM, CDTL, CDM PM) or transition into Data Standards/Programming.
Hands-on experience with modern CDM technologies: Learn RAVE, Veeva EDC, and AI-enabled workflows for data quality and analysis.
Why Join Thermo Fisher Scientific
Thermo Fisher Scientific is a world leader in serving science, enabling clients to make the world healthier, cleaner, and safer. You will join a 90,000+ colleague global team, where your contributions to clinical research and patient safety are recognized and valued.
We provide a flexible work environment, award-winning learning programs, mentorship, and career development opportunities to help you grow professionally and personally.
Thermo Fisher Scientific is an Equal Employment Opportunity Employer, committed to diversity, equity, and inclusion.
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