Perform case intake of Individual Case Safety Reports (ICSRs) from various sources (patients, healthcare professionals, literature, etc.). Enter and update safety data accurately in pharmacovigilance databases. Conduct initial assessment and triage of reported adverse events. Assist in coding medical terms…
Support the setup, initiation, and monitoring of clinical trials. Assist in preparing essential documents, trial master files (TMF), and regulatory submissions. Help coordinate communication between sponsors, sites, and vendors. Participate in site selection and qualification visits under supervision. Ensure data…
Assist in setting up, initiating, monitoring, and closing clinical study sites. Support in preparing essential documents (Trial Master File, Investigator Site File, etc.). Verify that data entered in case report forms (CRFs) is accurate and complete. Ensure site compliance with…
Collect, review, and process adverse event reports from clinical trials and post marketing sources. Perform data entry of case details into safety databases accurately and within timelines. Assist in coding adverse events, medical history, and medications using MedDRA and WHO…
Identify and develop new business opportunities through networking, cold calling, and client meetings. Present and promote company products or services to potential customers. Build and maintain strong, long lasting customer relationships. Meet or exceed monthly and quarterly sales targets. Prepare…
Review patient charts and clinical documents to identify diagnoses, procedures, and services provided. Assign accurate ICD 10 (International Classification of Diseases), CPT (Current Procedural Terminology), and HCPCS (Healthcare Common Procedure Coding System) codes to each diagnosis and procedure. Ensure codes…
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…