Clinical Documentation Specialist

Clinical Research Document SpecialistAs a Clinical Research Document Specialist, you will play a pivotal role in developing high-quality clinical trial documents that support drug development and approval processes.We are seeking an experienced professional to join our team in creating key clinical trial documents, including protocols, Investigator's...

Job Summary\As a Senior Clinical Data Coordinator, you will be responsible for managing clinical data with the utmost care and attention to detail. This role involves ensuring accuracy and integrity in project-specific documents and collaborating closely with project teams to facilitate document tracking and control activities.\Key...

We are seeking a Quality Assurance professional to provide day-to-day support across ongoing clinical trials.Key Responsibilities:Deliver QA expertise during study calls, including protocol deviation meetings and risk-based quality management discussions.Develop, review, update, and format standard operating procedures (SOPs) and other quality...

Medical Reviewer - Clinical ExpertAn exciting opportunity has arisen for a Medical Reviewer with expertise in clinical evaluation and risk management.

Job OpportunityWe are seeking a highly skilled Medical Scribe to join our team and contribute to the efficient management of medical records.The ideal candidate will have experience working with Electronic Health Record (EHR) systems, utilizing their technical expertise to accurately transcribe clinical notes into EMR/Billing systems.Key...

Job Title:Clinical Data Configurator">Job Description:Create and/or review derive data specifications as per the standards for SDTM, ADaM datasets and pooled analysis (ISS/ISE) datasets.Perform development and validation of analysis dataset, tables, listings and figures for both safety and efficacy parameters.Understand and comply with ICH-GCP guidelines,...

Job DescriptionWe are seeking a skilled clinical systems tester to support testing and validation activities in decentralized clinical trial environments.This role involves authoring and executing test scripts in Veeva EDC, aligned with protocol requirements. The successful candidate will be responsible for validating workflows across eCOA and IRT...

Lead Clinical Expert - Pharmacovigilance and Drug SafetyWe are seeking an experienced Senior Lead Clinical Expert to oversee our medical review teams and provide expert guidance on clinical and post-marketing drug safety. The successful candidate will have a strong understanding of GVP, GCP, FDA, and regulatory requirements related to drug safety.Clinical...

About the RoleWe are seeking an accomplished Technical Documentation Specialist to collaborate with our team. The ideal candidate will have a solid background in technical writing, preferably in the networking/telecommunications/contact center domains, and experience with DITA/Oxygen tools.The successful candidate will possess 8+ years of experience in...

As a seasoned healthcare professional with fluency in Telugu, you will be conducting clinical trial screening interviews for our esteemed clients.Job RequirementsCollaborate with our team to conduct thorough and efficient screening interviewsDemonstrate exceptional communication skills to ensure seamless interaction with candidatesMaintain accurate records...