Responsible for the drug surveillance program including the necessary follow-up, risk assessment, and relatedness to product on adverse reaction reports, oversight of safety in clinical trials and post marketing programs
This position is responsible for coding, chart compliance, and coding denial resolution. The ideal candidate will have CPC Certification and 2+ years’ experience in a hospital, surgical and medical office setting.
Discussing and reviewing patients medical history, symptoms, allergies, and current medications. Asking patients situation-specific questions to formulate accurate diagnoses. Formulating suitable treatment plans to address non-threatening conditions
Urgent opening in a leading brand company @Telangana
Company Details:Our client provides health care products and services. The Company offers primary as well as tertiary healthcare services. They also offers cardiac care, neurology, nephrology, and
Experience: • Associate – Min.12 months of AR follow up experience preferably in Hospital if not, physician RCM • Sr. Associate – Min.24 months of AR follow up experience preferably in Hospital if not, physician RCM • SME – Min. 4 years’ experience i
Carrying out pharmacovigilance activities on a product or group of products, including single case review, aggregate reporting, literature screening, signal detection and evaluation, in accordance with client’s guidelines and international regulation
1.Good domain knowledge in various functional areas such as Utilization Management, Care / Disease Management, Health & Wellness program Management, PHM (Population Health Management) etc.
2.Good knowledge in URAC / NCQA standards, HEDIS performance
Job Description :
The position is responsible for performing medical review of Individual Case Safety Reports (ICSRs), conducting medical assessement of all safety related data and ensuring medical accuracy of the ICSR narrative, coding a