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Associate Patient Data Specialist

Thermo Fisher Scientific
Thermo Fisher Scientific
0.6-1 years
Not Disclosed
10 Oct. 8, 2025
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/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

Associate Patient Data Specialist

Location: Remote, India
Job Type: Full Time
Category: Clinical Research – Fully Remote
Job Id: R-01330237


About the Role

Our Clinical Research team at PPD® is at the forefront of bringing cures to market, leveraging high-level scientific and clinical expertise to develop drugs for the world’s most challenging health concerns. The Associate Patient Data Specialist plays a critical role in assessing and managing subject data, collaborating across study teams and departments to ensure optimal trial outcomes.


Work Schedule

  • Standard: Monday to Friday

  • Work Environment: Office


Key Responsibilities

  • Independently perform critical assessments of subject data and collaborate with study teams to determine best approaches for data management.

  • Lead interdepartmental discussions to explore strategies and best practices tailored to trial-specific needs.

  • Review subject data from multiple sources with a data-analytic mindset; identify trends, risks, gaps, and opportunities for optimization.

  • Prepare and analyze clinical trial patient datasets and provide concise updates to study teams and stakeholders.

  • Adapt to evolving trial requirements and continuously update processes.

  • Enhance professional knowledge and skills in programming, technology, clinical trials, and the pharmaceutical industry through mentoring, presentations, and contributing to department policies and best practices.

  • Develop a thorough understanding of protocol schedules, EDC systems, contracts, budgets, and payment terms.

  • Escalate and assist in resolving performance issues involving clinical, site payments, or IT teams.

  • Lead internal team meetings and provide updates on subject data statuses.

  • Manage escalations with project teams, sites, and sponsors related to tracking system setup or maintenance issues.


Qualifications & Experience (Desired)

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

  • Experience:

    • Prior clinical research experience (6 months–1 year) is a plus.

    • Experience in process development or improvement (6 months–1 year) is a plus.

    • Experience in data assessments, analytics, or critical evaluations (6 months–1 year) is a plus.

  • Highly independent with the ability to lead multidisciplinary discussions.

  • Comfortable making decisions and maintaining proper documentation.

  • Able to work under continuous pressure and adapt to changing priorities.

  • Experience with scientific databases is a plus.


Skills & Competencies

  • Strong understanding of database structures and complex data systems.

  • Proficient in Microsoft Excel and capable of data capture and review.

  • Ability to provide quality control support with attention to detail.

  • Strong problem-solving skills.

  • Excellent written and verbal communication skills in English.

  • Ability to organize and manage multiple assignments within challenging timelines.

  • Adaptable and flexible with changing priorities.

  • Positive attitude, initiative, and self-motivation.

  • Ability to work collaboratively in a team environment.