Senior Clinical Document Specialist

Job Title: Clinical Documentation SpecialistAbout the RoleWe are seeking a highly skilled and experienced clinical documentation specialist to join our team. The ideal candidate will have a strong background in clinical document management, with experience in leading and planning migrations.Drive the implementation of CDGM initiatives, projects, and process...

Job OverviewWe are seeking a skilled Regulatory Writer to join our team. The successful candidate will be responsible for authoring and reviewing high-quality clinical and safety documents, including non-registration Clinical Study Reports (CSR), Development Safety Update Reports (DSUR), and Risk Management Plans (RMP).As a key member of the Clinical Trial...

Job Title: Clinical Documentation ManagerJob DescriptionWe are seeking a skilled and experienced Clinical Documentation Manager to join our team. In this role, you will be responsible for managing clinical documentation for various projects, including in-licensing, out-licensing, acquisitions, and divestments.Key Responsibilities:Act as the point of contact...

Job Title: Document Management Specialist">Process clinical study documents in accordance with client and project requirements, adhering to SOPs/WPs and relevant regulations.Liaise with project teams and other staff to ensure effective fulfillment of responsibilities.Complete assigned projects within specified timelines, ensuring adherence to regulatory...

Clinical Documentation Specialist Role:We are seeking a skilled Clinical Documentation Specialist to join our team. In this critical role, you will review clinical documentation in electronic health records to ensure accuracy, completeness, and compliance with coding standards.Key Responsibilities Include:Conduct concurrent reviews of inpatient records using...

Medical Writer Role">This is a Medical Writer role in the development and review of clinical and regulatory documents. The responsibilities include writing and reviewing various documents, ensuring adherence to established guidelines and regulations.ResponsibilitiesWrite and review clinical/regulatory documents such as clinical trial protocols, clinical...

Thryve Digital Health LLP is an emerging global healthcare partner that delivers strategic innovation, expertise, and flexibility to its healthcare partners. Being a US healthcare conglomerate captive, we have direct access to deeper insights that help us accelerate our learning process and keeps us ahead of the curve. Thryve delivers next-generation...

Thryve Digital Health LLP is an emerging global healthcare partner that delivers strategic innovation, expertise, and flexibility to its healthcare partners. Being a US healthcare conglomerate captive, we have direct access to deeper insights that help us accelerate our learning process and keeps us ahead of the curve. Thryve delivers next-generation...

Department: Revenue Cycle Management/Clinical Documentation ImprovementReports To: CDI Manager/DirectorSummary:The Senior CDI Specialist is responsible for leading clinical documentation improvement efforts to ensure accurate and complete medical record documentation that supports appropriate coding, reimbursement, and quality reporting. This role requires...

Clinical Documentation Reviewer: The **Clinical Documentation Review** and **Clinical Documentation Specialist** is a onsite position responsible for ensuring the accuracy and completeness of provider documentation in electronic health records. This role involves interpreting clinical information and communicating with physicians to resolve conflicting,...