Role & responsibilities :

- Enter clinical-trial data into EDC/eCRF systems accurately and within defined timelines.
- Review source documents and capture patient demographics, visit details, medical history, medications, vitals, lab values, procedures, and outcome details.
- Perform first-level quality checks for completeness, consistency, and formatting.
- Identify missing or unclear information and raise documentation queries.
- Update clinical forms based on source documents and study instructions.
- Support eSource and EDC workflows by ensuring accurate transfer of clinical information.
- Maintain documentation logs, query trackers, and data-entry status reports.
- Assist clinical reviewers and data managers in resolving documentation issues.
- Follow protocol-specific instructions, SOPs, GCP requirements, and data privacy standards.
- Ensure patient and study data confidentiality.
- Support AI-assisted data extraction workflows by validating and correcting system-generated entries.





Preferred candidate profile :

- Basic understanding of medical terminology, drugs, diseases, lab tests, and clinical documentation.
- Good typing speed and high data-entry accuracy.
- Strong attention to detail.
- Ability to read prescriptions, lab reports, discharge summaries, and clinical notes.
- Basic knowledge of MS Excel, Google Sheets, and web-based healthcare applications.
- Valuable written English.
- Ability to follow instructions, checklists, and standard operating procedures.

Eligibility :

- B.Pharm or M.Pharm graduates.
- Freshers can apply.
- Candidates with experience in clinical data entry, medical records, clinical research, medical transcription, medical scribing, pharmacovigilance, or healthcare documentation will be preferred.
- Basic computer knowledge is mandatory.

📌 Clinical Documentation Entry Associate (Telangana)
🏢 TrialBridge India
📍 Telangana