Clinical Documentation Expert

Clinical research is an exciting field that requires a structured approach. As a Clinical Research Associate, you will be responsible for coordinating clinical trial activities and ensuring compliance with international guidelines.Key Responsibilities:Assist with on-site coordination of clinical trial activities under supervisionMaintain essential documents,...

Job Title:Senior Clinical Data CoordinatorAbout This Role:This role involves project-specific and departmental document tracking and control activities, ensuring seamless collaboration among stakeholders. You will review CRF (as per protocol) and project-specific documents, initiate project-specific DMTMF (Data Management Trial Master File) and e-filing, and...

Job Summary:We are seeking a Clinical Operations Expert to oversee global clinical teams and provide technical support for clinical operations.Develop and implement strategies to meet recruitment targets.Collaborate with the team to create a project risk mitigation plan and manage clinical risks throughout the project lifecycle.Identify quality standards,...

**AI Digital Health Care Transformation**We are seeking a highly skilled clinical expert to support the development of our innovative AI digital health and medical device platform.This is a unique opportunity to shape the future of digital addiction and neurological care, improving diagnosis, treatment adherence, and engagement at scale.\Preferred...

Job Opportunity:Project Leadership PositionThis position involves leading end-to-end clinical reporting projects with a focus on timely and high-quality delivery.Key ResponsibilitiesDevelop, implement and manage clinical reporting projects using R programming language.Design, develop and maintain Shiny dashboards, internal tools and reusable...

**Job Title:** Clinical Quality Assurance SpecialistWe are seeking an experienced Clinical Quality Assurance Specialist to provide day-to-day support across ongoing clinical trials. This individual will play a key role in guiding study teams, maintaining compliance with Good Clinical Practice (GCP), and ensuring quality oversight.Key Responsibilities:Serve...

Senior Statistical ProgrammerSponsor-dedicated:You'll be at the heart of a global pharmaceutical company's innovation, driving the next generation of patient treatment where individuals are empowered to work with autonomy and ownership. This is an exciting time to be part of this new program.Position Overview:Leverage your advanced SAS programming skills and...

About Us:We are seeking a skilled Technical Writer to join our team. You will be responsible for creating clear, concise, and accurate documentation for products, services, and processes.Key Responsibilities:Develop comprehensive documentation including user manuals, API guides, knowledge base articles, internal process documentation, release notes, and...

A Medical Transcriptionist is responsible for listening to voice recordings made by doctors, nurses and other healthcare professionals. They convert these into accurate written medical reports and documents.Transcription of Medical Dictations: Listen to audio instructions of medical notes, consultations, discharge summaries, operative reports etc., and type...

Project Manager OpportunityAs a senior manager, you will lead clinical reporting projects from start to finish, utilizing R programming skills. This involves overseeing package development, Shiny app creation at an enterprise level, and designing and managing dashboards and internal tools.Key responsibilities include guiding SAS-to-R migration, translating...