Clinical Research Documentation Specialist

Clinical Research Document Expert">We are seeking a skilled Clinical Research Document Expert to join our team. This individual will be responsible for creating and analyzing clinical trial documents, working with key clinical documents such as protocols, informed consent forms, and clinical study reports.">Key Responsibilities:Author and analyze clinical...

Job Title: Clinical Coding SpecialistDescription:We are seeking a skilled Clinical Coding Specialist to join our team. As a Clinical Coding Specialist, you will be responsible for reviewing and interpreting complex medical reports to assign accurate codes for procedures and diagnoses.

Job Position: QA SpecialistAbout the RoleWe are seeking a highly motivated and detail-oriented Quality Assurance (QA) Specialist to join our team.The successful candidate will be responsible for ensuring compliance with Good Clinical Practice (GCP) and internal quality standards.Key ResponsibilitiesProvide QA support to clinical study teams, performing...

Job Title:Clinical Coding SpecialistAbout the Role:The Clinical Coding Specialist is responsible for assigning accurate and appropriate codes to medical procedures and diagnoses.This involves reviewing patients' charts and documents, ensuring compliance with government and insurance regulations, and maintaining up-to-date knowledge of medical coding...

Clinical Research Associate RoleWe are offering an exciting opportunity for fresh graduates to launch their careers in clinical research.Assist with on-site coordination of clinical trial activities under supervision and mentorshipMaintain essential documents, site files, and case report forms accuratelySupport the investigator in protocol compliance and...

Job OverviewWe are seeking a skilled Senior Clinical Data Coordinator to join our team. The ideal candidate will have strong experience in clinical data management and be able to manage multiple projects simultaneously.About the RoleThis is a full-time role that involves coordinating clinical trials, managing documents, and ensuring data quality.The Senior...

Immunodiagnostics Documentation SpecialistJob Title: Immunodiagnostics Documentation SpecialistLocation: Remote (Hybrid)Role Overview:We are seeking a skilled Documentation Specialist to develop and maintain clear, accurate, and compliant documentation for immunodiagnostic products, including IFUs, user manuals, product labels, and digital learning aids.Key...

Job DescriptionAs a critical evaluator of AI responses, your primary responsibility will be to assess the usefulness and quality of generated content. This involves evaluating literature summarization, clinical question answering, and decision support.With expertise in respective disciplines, you will score AI responses across 10 key criteria using a Likert...

Job Title: Medical Record Coordinator">The Medical Record Coordinator is responsible for ensuring the accuracy and completeness of patient medical records. This role involves reviewing physician dictation, transcribing clinical notes into EMR/Billing systems, and preparing medical record documentation/charts for physician review.">Key Responsibilities...

Job Opportunity: Clinical Systems TesterThis role requires a flexible and skilled individual to support testing and validation activities within a Decentralized Clinical Trial (DCT) environment.Key Responsibilities:Author and execute test scripts in Veeva EDC, aligned with protocol requirements for accurate data capture and management.Validate workflows...