Instagram
youtube
Facebook

Associate Patient Data Specialist

0-2 years
₹4 – ₹6 LPA
10 July 29, 2025
Job Description
Job Type: Full Time Education: B.Tech/B.Sc./M.Sc./B.Pharm/M.Pharm/Life science 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

Associate Patient Data Specialist
Location: Bangalore, Karnataka, India (Fully Remote)
Job ID: R-01322344
Job Type: Full-time
Department: Clinical Research
Shift: Standard (Monday to Friday)
Estimated Salary: ₹4 – ₹6 LPA (based on entry-level CRO roles in data analytics)


Role Summary:
Thermo Fisher Scientific is hiring an Associate Patient Data Specialist to support its PPD® clinical research division. This remote-based role focuses on reviewing, analyzing, and managing patient-level clinical trial data from multiple sources. You’ll play a key part in optimizing trial outcomes by detecting data trends, inconsistencies, and opportunities for process improvement, while contributing to the overall clinical operations.


Key Responsibilities:

  • Perform critical assessments of patient subject data across multiple clinical trial platforms

  • Identify trends, gaps, and data anomalies with an analytics-driven mindset

  • Collaborate with cross-functional teams and lead discussions on data strategy and optimization

  • Understand trial protocol schedules, events, procedures, EDC systems, budgets, and contracts

  • Provide data insights and updates to study teams, ensuring concise and accurate communication

  • Monitor tracking system performance and manage escalations with teams and stakeholders

  • Generate documentation and reports, contributing to continuous improvement of data processes

  • Support internal audits and ensure compliance with GCP and data documentation standards


Qualifications & Desired Experience:

  • Bachelor’s degree in Life Sciences, Engineering, Biostatistics, Programming, or related fields

  • Prior experience (6 months to 1 year) in:

    • Clinical research or related healthcare analytics

    • Process development or optimization

    • Data assessments or analytical reviews

  • Independent thinker with the ability to lead multidisciplinary discussions

  • Understanding of clinical trial structure and terminology is an advantage


Required Skills:

  • Proficiency in Microsoft Excel and complex database structures

  • Strong attention to detail and critical thinking ability

  • Excellent communication (written and verbal) and interpersonal skills

  • Strong time and task management with the ability to adapt to shifting priorities

  • Self-motivated with a proactive approach to problem-solving

  • Ability to perform quality control checks and ensure data integrity


Why Join Thermo Fisher Scientific?

  • Work in a global CRO environment on meaningful research projects

  • Gain cross-functional exposure and grow professionally

  • Enjoy a fully remote work culture

  • Be part of an organization committed to a healthier, cleaner, and safer world