Clinical Document Specialist

Job Title: Regulatory Documentation SpecialistJob Summary:To write, review and manage the production of high quality clinical and safety documentation for submission to regulatory authorities in support of marketing applications.Main Responsibilities:• Author, review and independently manage high quality clinical and safety documents, including Clinical...

Role & responsibilitiesHandle, organize, and maintain clinical, medical, and healthcare project documentation.Accurately enter and validate healthcare and research data in internal systems.Review medical case records, lab reports, and related documentation for completeness.Collaborate with research, operations, and regulatory teams to gather required...

**Clinical Documentation Improvement (Inpatient ) - 10 resources,** Requirement: a. Must have at least 5 years of IPDRG coding experience and b. CDIP certification c. Understand MS-DRG and Inpatient Prospective Payment System Clinical documentation improvement (CDI) is the process of reviewing medical record documentation for completeness and accuracy....

Job Description:As a Clinical Document Authoring specialist, you will be responsible for crafting and analyzing clinical trial documents. Your expertise will ensure the accuracy and clarity of these critical documents.The ideal candidate will have in-depth knowledge of clinical trial phases, study design, and drug development. You will work with key clinical...

Job Description:We are seeking a detail-oriented and organized Trial Master File Specialist to join our team. The ideal candidate will have 1-15 years of experience in TMF management, with strong knowledge of clinical study documents and excellent communication skills.As a Trial Master File Specialist, you will be responsible for:Processing study documents...

Medical Content SpecialistWe are seeking a detail-oriented and skilled Medical Content Specialist to assist in the creation, editing, and coordination of clinical/regulatory documents. This role requires excellent writing, editing, and communication skills, as well as the ability to work effectively within a team.Responsibilities: Compile, write, and edit...

About UsWe help clients modernize their technology infrastructure, adopt cloud and AI solutions, and accelerate innovation.Our team combines deep industry expertise with agile development practices, enabling scalable and cost-effective digital transformation.Key Responsibilities:Author and analyze clinical trial documents.Work with key clinical documents:...

**Job Title-** Clinical Documentation Improvement (Inpatient ) **Requirement**: - Must have at least 5 years of IPDRG coding experience and - CDIP certification - Understand MS-DRG and Inpatient Prospective Payment System **Role -** - Clinical documentation improvement (CDI) is the process of reviewing medical record - documentation for completeness and...

Job Title: TMF SpecialistAs a key member of our team, you will be responsible for processing study documents in accordance with client and study requirements, adhering to SOPs and relevant regulations. This role involves close collaboration with study teams and other TMF staff to ensure effective fulfillment of responsibilities.The successful candidate will...

Job DescriptionDescriptionClinical Operations SpecialistSyneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities.Our Clinical Development model brings the customer and the...