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Clin Data Assoc I

Thermo Fisher Scientific
Thermo Fisher Scientific
1-1.6 years
Not Disclosed
10 Jan. 1, 2026
Job Description
Job Type: Full Time Remote Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Clinical Data Associate I (CDA I) – Remote, India

Company: Thermo Fisher Scientific
Job Type: Full-Time, Fully Remote
Location: India (Remote)
Experience: 1 – 1.6 years
Category: Clinical Research / Data Management


About Thermo Fisher Scientific

Thermo Fisher Scientific is a global leader in serving science, delivering innovative technologies and solutions that enable life sciences research, analytical problem-solving, diagnostics, and laboratory efficiency. With a workforce of over 90,000 employees worldwide and annual revenue exceeding $44 billion, Thermo Fisher supports the discovery and delivery of life-changing medicines and solutions.

Learn more: www.thermofisher.com


Role Overview

The Clinical Data Associate I is responsible for entry-level clinical data cleaning, reconciliation, and query resolution to maintain data integrity in accordance with GCP, SOPs/WPDs, and study protocols. This role involves collaboration with global study teams to ensure accurate, timely, and inspection-ready clinical data throughout the study lifecycle.


Key Responsibilities

  • Identify, track, and resolve data discrepancies in EDC systems (RAVE / Veeva).

  • Implement CRF designs in designated graphic design packages as needed.

  • Generate, track, and resolve data clarifications and queries efficiently.

  • Ensure adherence to GCP guidelines, global SOPs, and project protocols.

  • Collaborate with cross-functional study teams to ensure high-quality, accurate, and timely study data.

  • Maintain confidentiality of clinical and proprietary client data.

  • Contribute to inspection-readiness and audit support for clinical studies.


Qualifications & Skills

  • Education: Bachelor’s degree or equivalent in Life Sciences or related field.

  • Experience: 1 – 1.6 years in clinical data management / data entry roles.

  • Technical Skills:

    • Experience with RAVE and/or Veeva EDC systems.

    • Strong analytical and problem-solving abilities.

    • Proficiency in Microsoft Office (Word, Excel, PowerPoint).

  • Soft Skills:

    • Excellent written and verbal communication in English.

    • Strong attention to detail and numerical accuracy.

    • Ability to work independently and in a team environment.

    • Good judgment and flexibility in decision-making.


Work Environment

  • Standard Mon-Fri work schedule.

  • Fully remote with occasional drives to site locations if required.

  • Office or clinical environment exposure may be needed occasionally.


Career Growth & Opportunities

  • FSP model exposure: Collaborate with a globally recognized biopharmaceutical client.

  • End-to-end study involvement: From data cleaning and reconciliation to study close-out.

  • Career pathways: Progress along Clinical Data Management track (Senior CDM, CDTL, CDM PM) or transition into Data Standards/Programming.

  • Hands-on experience with modern CDM tools, AI-enabled workflows, and global clinical trial technologies.