Collect, review, and process adverse event reports from healthcare professionals, patients, and clinical studies. Enter and maintain accurate case data in safety databases. Perform case assessment and narrative writing under supervision. Assist in the preparation of Individual Case Safety Reports…
Data Entry & Verification: Enter and validate clinical trial data into electronic systems. Data Cleaning: Identify and correct data discrepancies or inconsistencies. Database Support: Assist with the setup and maintenance of clinical trial databases (e.g., EDC systems). Documentation: Support the…
Assist in the preparation and coordination of clinical trial protocols and associated documents. Support the monitoring of clinical trials at various stages, including site initiation, maintenance, and close out. Ensure that study sites are compliant with Good Clinical Practice (GCP)…
Assist in the coordination and conduct of clinical trials under supervision Support patient recruitment, screening, and enrollment according to protocol criteria Schedule and manage patient visits, sample collection, and follow ups Collect and accurately enter data into Case Report Forms…
Assist in monitoring clinical trials at investigational sites under supervision Ensure compliance with ICH GCP guidelines, regulatory requirements, and company SOPs Support site initiation, routine monitoring, and close out visits Help in verifying source data and case report forms (CRFs)…
Prepare, review, and submit medical claims to insurance companies (electronically and paper). Verify patient insurance coverage and benefits. Follow up on unpaid or denied claims; initiate appeals or re submissions as necessary. Post payments and reconcile accounts accurately. Work with…
Assist in setting up, monitoring, and closing clinical trial sites under supervision. Ensure trials are conducted in compliance with protocols, ICH GCP guidelines, and regulatory requirements. Perform site visits (remote or on site) and assist with source data verification. Maintain…
Assist in the design, development, and testing of data collection tools (e.g., Case Report Forms/eCRFs). Perform data entry and data validation activities in clinical trial databases. Assist in query management and data cleaning activities under supervision. Support database lock and…