Welcome Back

Google icon Sign in with Google
OR
I agree to abide by Pharmadaily Terms of Service and its Privacy Policy

Create Account

Google icon Sign up with Google
OR
By signing up, you agree to our Terms of Service and Privacy Policy
Instagram
youtube
Facebook

Clin Data Assoc Ii

Thermo Fisher Scientific
Thermo Fisher Scientific
1.6-3 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 II (CDA II) – Remote, India

Company: Thermo Fisher Scientific
Job Type: Full-Time, Fully Remote
Location: India (Remote)
Experience: 1.6 – 3 Years
Category: Clinical Research / Data Management


About Thermo Fisher Scientific

Thermo Fisher Scientific is a global leader in serving science, providing innovative technologies and solutions for life sciences research, clinical trials, analytical challenges, diagnostics, and laboratory efficiency. With over 90,000 employees worldwide and annual revenue exceeding $44 billion, Thermo Fisher supports the development and delivery of life-changing medicines and scientific solutions.

Learn more: www.thermofisher.com


Role Overview

The Clinical Data Associate II is responsible for advanced clinical data review, cleaning, and reconciliation to ensure data integrity, timeliness, and inspection readiness across clinical studies. This role involves managing complex queries, performing SAE and third-party reconciliations, reviewing data listings, contributing to CRF design, and collaborating with cross-functional teams to deliver high-quality, analysis-ready datasets.


Key Responsibilities

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

  • Generate, monitor, and resolve data clarifications and queries.

  • Review data listings for accuracy and consistency; analyze validation outputs.

  • Perform Serious Adverse Event (SAE) and third-party vendor reconciliations.

  • Contribute to CRF design and database updates.

  • Produce project-specific status reports for stakeholders and CDM management.

  • Ensure compliance with GCP, SOPs, Data Validation Manuals, and project protocols.

  • Maintain confidentiality of clinical and proprietary client data.


Qualifications & Skills

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

  • Experience: 1.6 – 3 years in clinical data management or related roles.

  • Technical Skills:

    • Proficiency with RAVE and/or Veeva EDC systems.

    • Knowledge of clinical trial terminology and data management processes.

    • Strong analytical, problem-solving, and organizational skills.

  • Soft Skills:

    • Excellent written and verbal communication in English.

    • Attention to detail and numerical accuracy.

    • Ability to work independently and in team environments.

    • Flexibility, adaptability, and good judgment in decision-making.


Work Environment

  • Standard Monday–Friday schedule.

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

  • Office or clinical environment exposure may occur.


Career Growth & Opportunities

  • Global exposure: Work on international clinical trials across phases and therapeutic areas.

  • End-to-end ownership: Participate in study delivery from set-up to close-out.

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

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