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.
Andra Pradesh :
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China | Quarry Bay |Hubei :
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Brussels |Flemish Brabant :
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Sofia |Canada :
Canada |Ontario :
Richmond Hill | Mississauga | Uxbridge | North York | Renfrew | Australia |Quebec :
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Japan | Saitama |Tokyo :
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Brazil | Sao paulo |South America :
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Taipei |Williamson :
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