Clinical documentation specialist

Role & responsibilities :Review and summarize patient medical records and clinical notes.Ensure accuracy and completeness of clinical documentation.Collaborate with billing and coding teams for data clarification.Maintain confidentiality and adhere to HIPAA compliance.Meet daily quality and productivity targets.Learn and work efficiently on EHR/EMR...

OverviewVelocity Clinical Research is an owned and integrated research site organization, providing excellence in patient care, high quality data and fully integrated research sites. At Velocity, we align our values and behaviors to give our employees the best chance of delivering on our brand promise: to bring innovative medical treatments to patients. We...

Clinical Informatics Specialist – Rehabilitation Data &Health Standards IntegrationRole OverviewWe are seeking a Clinical Informatics Specialist with strong knowledge of ICD, ICF, and ICHIframeworks and hands-on exposure to rehabilitation assessment and therapy equipment.The candidate will act as a bridge between therapists, clinicians, and software...

Job title: Trainee Junior specialist- Electronic Documentation SpecialistLocation: HyderabadOpella is the self-care challenger with the purest and third-largest portfolio in the Over-The-Counter (OTC) & Vitamins, Minerals & Supplements (VMS) market globally.  Our mission is to bring health in people's hands by making self-care as simple as it should be. For...

Who we are?Shanghai United Imaging Healthcare Co., Ltd. is dedicated to providing, developing and producing high-performance advanced medical imaging, radiotherapy equipment, life science instruments and offers intelligent digital solutions to customers worldwide. UIH is committed to creating more value for our customers and constantly improving the global...

PlebC Innovations Pvt. Ltd. is looking for aClinical/Regulatory Affairs Specialistto join our growing team in Hyderabad.About the Role:You will be responsible for supporting clinical and regulatory operations, ensuring compliance with applicable guidelines, preparing documentation for regulatory submissions, and coordinating with authorities for approvals....

Role & responsibilitiesPrioritization and Prior Approval: Responsible for evaluating the patient's condition, determining the medical necessity, and submitting the necessary documentation to the insurance company for approval ensuring that the proposed treatment or service is covered by the insurance policy before it is performed.Medical Necessity...

At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You'll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world.A Day in the LifeResponsibilities may include the following and other duties may be assigned.Minimum of 4 years...

Principal Clinical Programmer (RAVE EDC)Statistics & Data Corporation (SDC), a specialized contract research organization (CRO) headquartered in Arizona, delivering top-tier clinical trial services to pharmaceutical, biologic, and medical device/diagnostic companies since 2005. SDC providing a technology enabled service offering to provide clients with both...

Role DescriptionThis is a full-time, on-site role for an Oncology Authorizations Specialist, based in Hyderabad. The Specialist will be responsible for securing prior authorizations for oncology services, liaising between healthcare providers and insurance companies, and ensuring compliance with organizational and payer guidelines. Tasks also include patient...