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Abstractor - Analyst

1-3 years
Not Disclosed
10 Dec. 2, 2025
Job Description
Job Type: Full Time 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

Abstractor – Analyst (Real World Evidence)

Location: Bengaluru, Karnataka, India
Job Type: Contract | Onsite
Job ID: P-100727**

About the Role

The Abstractor – Analyst will support Real World Evidence (RWE) operations through accurate data abstraction, data quality verification, and clinical documentation review. This role is critical in driving high-quality RWE insights for healthcare, life sciences, pharmaceutical, and research organizations. The position requires strong analytical skills, attention to detail, and the ability to interpret clinical and scientific information with precision.

This contract-based role is ideal for professionals with experience in clinical data abstraction, medical coding, or RWE analytics who are looking to contribute to evidence generation that supports regulatory, clinical, and commercial decision-making.


Key Responsibilities

  • Extract, abstract, and validate clinical and non-clinical information from medical records and structured/unstructured data sources.

  • Perform quality checks on abstracted data to ensure accuracy, completeness, and compliance with project requirements.

  • Support development of RWE datasets by applying predefined abstraction rules and documentation standards.

  • Review source documents such as EMRs, case files, clinical notes, and diagnostic records to identify relevant patient information.

  • Collaborate with cross-functional teams including data management, epidemiology, medical writing, and analytics.

  • Maintain up-to-date knowledge of clinical terminologies, disease areas, and documentation standards applicable to the project.

  • Ensure adherence to timelines, workflow processes, and quality benchmarks.

  • Assist in the preparation of reports, documentation summaries, and project tracking materials as required.

  • Manage sensitive patient data with strict adherence to confidentiality, privacy regulations, and organizational compliance guidelines.


Required Qualifications & Experience

  • Bachelor’s or Master’s degree in Life Sciences, Pharmacy, Nursing, Biotechnology, Medical Science, or a related discipline.

  • 1 to 3 years of experience in clinical data abstraction, RWE processes, clinical data management, medical coding, or similar roles within healthcare, pharmaceutical, or CRO environments.

  • Strong understanding of clinical terminologies, medical records, EMRs/EHRs, and disease classifications (ICD, SNOMED, CPT preferred).

  • Proficiency in interpreting scientific and clinical documentation.

  • Excellent attention to detail with strong analytical and problem-solving skills.

  • Working knowledge of regulatory standards and clinical data handling best practices.

  • Ability to work onsite and manage workload in a structured, deadline-driven environment.


Preferred Skills

  • Experience supporting Real World Evidence or observational study projects.

  • Familiarity with medical coding systems, abstraction tools, or clinical documentation software.

  • Knowledge of epidemiology, clinical research methodologies, or evidence generation frameworks.

  • Strong written and verbal communication skills.

  • Ability to collaborate effectively with cross-functional teams.


Experience Level

Intermediate (1–3 years experience required) in RWE, clinical data abstraction, medical coding, clinical research, or related functions.