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Clin Data Assoc I

Thermo Fisher Scientific
Thermo Fisher Scientific
1-1.6 years
preferred by company
10 Jan. 7, 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)

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


Job Overview

Thermo Fisher Scientific is hiring a Clinical Data Associate I (CDA I) to support global clinical research programs through accurate and compliant clinical data management activities. This entry-level role is ideal for professionals with foundational experience in clinical data cleaning, reconciliation, and EDC systems, who are looking to grow within a world-class Contract Research Organization (CRO) environment.

As part of the PPD® Clinical Research Services team, you will contribute to high-impact clinical trials supporting leading pharmaceutical and biotechnology companies worldwide.


Key Responsibilities

  • Perform clinical data cleaning and reconciliation activities with high accuracy.

  • Identify, review, resolve, and document data discrepancies in clinical databases.

  • Generate, track, and resolve data queries and clarifications in a timely manner.

  • Update and maintain clinical data in EDC systems in compliance with study protocols.

  • Support CRF design implementation using approved graphical design tools, when required.

  • Collaborate with cross-functional study teams to ensure data integrity and inspection readiness.

  • Ensure adherence to GCP guidelines, SOPs/WPDs, and regulatory requirements throughout the study lifecycle.

  • Maintain strict confidentiality of clinical and proprietary client data.


Experience Requirements

  • 1 to 1.6 years of hands-on experience in Clinical Data Management (CDM) or related clinical research roles.

  • Prior experience working with RAVE and/or Veeva EDC systems is mandatory.


Educational Qualifications

  • Bachelor’s degree or equivalent qualification in life sciences, pharmacy, biotechnology, clinical research, or a related discipline.


Required Skills & 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 systems and clinical databases.

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

  • Good problem-solving and decision-making abilities.

  • Ability to work effectively under direct supervision as well as independently.

  • Proven ability to work collaboratively in a global team environment.

  • Strong commitment to quality, compliance, and data integrity.

  • Flexibility and adaptability in a fast-paced clinical research setting.


Working Conditions

  • Work is primarily performed in an office or remote clinical research environment.

  • Occasional travel to study or site locations may be required, based on project needs.


Career Growth & Development

This role supports a dedicated Functional Service Provider (FSP) model for a globally recognized biopharmaceutical client known for innovation in specialty medicines, vaccines, and advanced therapeutics.

As a CDA I, you will:

  • Collaborate with global data science and clinical teams on high-visibility studies.

  • Gain exposure to end-to-end clinical data management, from study setup to close-out.

  • Access structured learning pathways, mentorship, and stretch assignments.

  • Build long-term career paths in Clinical Data Management (Senior CDM, CDTL, CDM Project Manager) or transition into Data Standards, Programming, or Advanced CDM roles, based on performance and business needs.


Why Join Thermo Fisher Scientific

  • Work on global, multi-phase clinical trials across diverse therapeutic areas.

  • Gain hands-on experience with modern EDC platforms, data quality frameworks, and AI-enabled CDM workflows.

  • Strengthen analytical, project management, and risk management skills in a global delivery model.

  • Be part of a mission-driven organization dedicated to improving patient outcomes worldwide.


About Thermo Fisher Scientific

Thermo Fisher Scientific Inc. is the world leader in serving science, with annual revenue exceeding USD 44 billion. With more than 90,000 colleagues globally, the company enables customers to make the world healthier, cleaner, and safer through innovative technologies, services, and pharmaceutical solutions.

Thermo Fisher Scientific is an Equal Employment Opportunity Employer and values diversity, inclusion, and merit-based career growth.


Apply Now

If you are passionate about clinical data management and want to contribute to life-changing research on a global scale, apply now and advance your career with Thermo Fisher Scientific.