Clinical Documentation Specialist

Job Title: Clinical Support SpecialistWe are seeking a highly organized and detail-oriented Clinical Support Specialist to join our team. In this role, you will be responsible for handling templated clinician/clinic communications, maintaining accurate records, and performing daily logs.This is a repetitive, SOP-driven back-office role that requires minimal...

Job Title:Clinical Research Associate">Job Description:">Author and analyze clinical trial documents.">Work with key clinical documents: Protocol, Informed Consent Form, Clinical Study Report, Summary of Clinical Safety/Efficacy, Access Evidence Dossier, Statistical Analysis Plan and more.">Create, validate, and refine prompts for AI-assisted document...

Job Title: Quality Assurance ProfessionalWe are seeking an experienced Quality Assurance (QA) Specialist to provide day-to-day clinical quality assurance support across ongoing clinical trials. Main Responsibilities:Serve as the primary QA support resource for clinical study teams, ensuring compliance with Good Clinical Practice (GCP) and internal quality...

Medical Scribe SpecialistWe are seeking a highly skilled Medical Scribe Specialist to join our team. This role requires exceptional administrative and technical skills to effectively support our providers.The ideal candidate will have 3-5 years of experience as a Live Medical Scriber and possess strong organizational and communication skills. They will be...

Job TitleClinical Specialist in Heart InterventionAbout the RoleWe are seeking a skilled and experienced Clinical Specialist in Heart Intervention to join our medical team.Deliver high-quality patient care and treatment for cardiovascular conditionsPerform advanced procedures like coronary angioplasty and stent placement with precision and...

Are you a skilled medical writer and clinical study researcher seeking a new challenge? Look no further! We are currently looking for a talented professional to join our team as a Medical Writer/Clinical Study Researcher.Key Responsibilities:Developing High-Quality Clinical Trial Documents:ProtocolsInvestigator's Brochures (IBs)Informed Consent Forms...

Job Overview:The role of a medical scribe is a vital part of healthcare documentation. In this position, you will work closely with our team to ensure timely and accurate recording of patient visits.Responsibilities:You will review and transcribe physician dictation into clinical notes within electronic medical records (EMR) and billing systems.You will...

Job OverviewThe role of Nuclear Medicine Imaging Scientist is a critical position within our organization. This individual will be responsible for reviewing imaging data, ensuring technical adequacy, and providing medical writing support at a clinical trial level.Main ResponsibilitiesPerform technical quality review of images per trial specificationsPerform...

About Client:Our Client is a global IT services company headquartered in Southborough, Massachusetts, USA. Founded in 1996, with a revenue of $1.8B, with 35,000+ associates worldwide, specializes in digital engineering, and IT services company helping clients modernize their technology infrastructure, adopt cloud and AI solutions, and accelerate innovation....

Key Clinical Data Configurator RoleA Clinical Data Configurator plays a vital role in ensuring the accuracy and quality of clinical data. The primary responsibilities include creating and reviewing data specifications, performing analysis dataset development and validation, and maintaining compliance with regulatory guidelines.Essential...