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Clin Data Assoc I

Thermo Fisher Scientific
Thermo Fisher Scientific
1-1.6 years
preferred by company
10 Jan. 26, 2026
Job Description
Job Type: Full Time Remote Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ 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

Job ID: R-01338259
Job Type: Full-Time
Work Mode: Fully Remote
Category: Clinical Research / Clinical Data Management
Location: India (Remote)
Work Schedule: Monday to Friday

Job Overview

We are seeking a detail-oriented and motivated Clinical Data Associate I (CDA I) to join our growing Clinical Research Services team in India. This fully remote opportunity allows you to contribute to high-impact global clinical trials while working with a leading contract research organization (CRO) supporting top pharmaceutical and biotechnology companies worldwide.

As part of the PPD® Clinical Research portfolio under Thermo Fisher Scientific, you will play a critical role in ensuring data accuracy, integrity, and inspection readiness across all stages of the clinical trial lifecycle.

Role & Responsibilities

The Clinical Data Associate I is responsible for performing entry-level clinical data management activities in compliance with Good Clinical Practice (GCP), study protocols, and global SOPs/WPDs.

Key Responsibilities Include:

  • Identify, review, resolve, and update data discrepancies in clinical databases

  • Generate, track, and resolve data queries and data clarification forms (DCFs)

  • Perform data cleaning and reconciliation activities with high accuracy

  • Make required updates to data management systems in line with study requirements

  • Support CRF design and implementation using designated graphic design tools, when applicable

  • Collaborate with cross-functional study teams to ensure timely issue resolution

  • Maintain inspection-ready clinical data throughout the study lifecycle

Education & Experience Requirements

  • Bachelor’s degree or equivalent in Life Sciences, Pharmacy, Biotechnology, or a related field

  • 1 to 1.6 years of relevant clinical data management experience

  • Hands-on experience with RAVE and/or Veeva EDC systems is mandatory

Required Knowledge, Skills & Competencies

  • Strong understanding of clinical trial processes, GCP, and data validation standards

  • High attention to detail with strong numerical and analytical skills

  • Proficiency in interactive computer applications and clinical databases

  • Excellent written and verbal communication skills with strong command of English

  • Ability to follow global SOPs, regulatory guidelines, and client expectations

  • Strong problem-solving and decision-making capabilities

  • Ability to work effectively with supervision as well as independently

  • Proven ability to maintain confidentiality of clinical and proprietary data

  • Flexible, adaptable, and capable of working in a collaborative team environment

  • Working knowledge of study protocols and Data Validation Manuals

Working Conditions

  • Work is performed in a remote office-based environment

  • Occasional travel to site locations may be required, depending on study needs

Career Development & Growth

This role supports a dedicated Functional Service Provider (FSP) model for a globally recognized biopharmaceutical sponsor known for innovation in specialty medicines and vaccines. As part of this engagement, you will collaborate with global data science and clinical teams on high-visibility projects.

The FSP model promotes continuous professional development through structured learning paths, mentorship programs, and stretch assignments. Career progression opportunities include advancement within Clinical Data Management (Senior CDM, CDTL, CDM Project Manager) or transitions into Data Standards, Programming, or Advanced Data Analytics, based on performance and business needs.

Why Join Us

  • Contribute to life-changing medicines and global clinical research

  • Gain hands-on experience with modern CDM tools, EDC platforms, and AI-enabled workflows

  • Work on international clinical trials across multiple therapeutic areas and phases

  • Experience end-to-end study involvement from study setup through close-out

  • Enhance global project management, risk management, and data analysis skills

About Thermo Fisher Scientific

Thermo Fisher Scientific Inc. is a global leader in serving science, with annual revenues exceeding $44 billion. Our mission is to enable our customers to make the world healthier, cleaner, and safer. With a workforce of over 90,000 colleagues worldwide, we deliver innovative technologies, pharmaceutical services, and scientific solutions through industry-leading brands such as Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, and Patheon.

Thermo Fisher Scientific is an Equal Employment Opportunity employer and is committed to fostering a diverse and inclusive workplace.