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Associate Patient Data Specialist

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
Job Type: Full-time, Fully Remote
Job ID: R-01322344
Work Schedule: Standard (Monday to Friday)
Estimated Salary: ₹4 – ₹6 LPA (based on experience and market standards)


About the Role:
As an Associate Patient Data Specialist, you will play a key role in analyzing subject data for clinical trials, contributing to data-driven decisions in a high-caliber, global Contract Research Organization (CRO). You’ll be part of the PPD® clinical research portfolio, supporting the development of innovative drugs addressing global health challenges.


Key Responsibilities:

  • Perform critical data assessments independently and collaborate with study teams to determine best approaches to manage and interpret subject-level clinical data.

  • Review data from multiple sources with a data-analytic mindset to identify trends, risks, gaps, and areas for optimization as trials progress.

  • Prepare and analyze clinical trial datasets, adapting to evolving study needs and providing concise updates to stakeholders.

  • Lead internal discussions and multidisciplinary team meetings, handling escalations and resolving system-related issues.

  • Maintain a strong grasp of study protocols, schedules of events, EDC systems, contracts, and payment terms.

  • Assist with performance issue resolution, process improvements, and documentation aligned with best practices.

  • Support quality control, provide tracking system updates, and manage escalations related to tracking and data setups.


Desired Qualifications:

  • Bachelor’s degree in Life Sciences, Engineering, Biostatistics, Programming, or a related field.

  • Preferred 6 months to 1 year of experience in:

    • Clinical research

    • Data analysis or assessments

    • Process development or improvement

  • Familiarity with database structures and scientific data systems is an advantage.

  • Strong decision-making ability and documentation practices under changing priorities.

  • Comfortable working independently and collaborating across teams.


Essential Skills:

  • Understanding of complex database systems

  • Proficiency in Microsoft Excel

  • Attention to detail and analytical problem-solving

  • Ability to handle multiple projects and adapt to shifting timelines

  • Excellent verbal and written communication in English

  • Strong organizational, quality control, and stakeholder management skills

  • Proactive, self-motivated, and collaborative mindset


Why Join Us?

  • Contribute to a global CRO at the forefront of scientific discovery and drug development.

  • Be part of a dynamic and remote-friendly team with opportunities for learning and mentorship.

  • Gain diverse exposure to clinical trial operations and cutting-edge analytics.

  • Work in an environment that values initiative, innovation, and continuous learning.