Role & responsibilities :

- Review patient clinical information, medical history, medications, lab reports, vitals, diagnosis details, and visit notes.
- Assist in screening patients against study-specific inclusion and exclusion criteria.
- Identify missing, inconsistent, or unclear clinical information and raise queries for clarification.
- Support clinical data review in EDC/eCRF systems.
- Review source documents and ensure data entered into the system matches available clinical records.
- Assist in medical review of trial-related documents under senior supervision.
- Flag potential safety concerns, abnormal lab values, adverse events, or clinically relevant findings.
- Coordinate with clinical operations, data entry, pharmacovigilance, and study teams.
- Maintain confidentiality of patient and study-related data.
- Follow SOPs, study protocols, GCP guidelines,



and internal quality standards.
- Support AI-assisted review workflows by verifying system-generated outputs before final use.

Preferred candidate profile :

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

Training Provided :

Selected candidates will receive training on clinical-trial workflows, protocol review, EDC/eCRF review, patient screening, data quality checks, documentation standards, and TrialBridge.ai platform workflows.

📌 Clinical Reviewer (Telangana)
🏢 TrialBridge India
📍 Telangana