Clinical Documentation Specialist Lead

Medical Writer/Clinical Study Researcher Job SummaryWe are seeking a highly skilled Medical Writer/Clinical Study Researcher to join our team. As a key member of our clinical research team, you will be responsible for developing high-quality key clinical trial documents, including protocols, Investigator's Brochures (IBs), Informed Consent Forms (ICFs), Case...

Senior Medical Advisor - Clinical Phase and Pharmacovigilance ExpertWe are seeking a seasoned Senior Medical Advisor to lead our clinical and pharmacovigilance teams. As a medical professional with a strong track record in drug safety, you will provide expert guidance, review protocols, and develop medical monitoring plans.Clinical Phase:Provide medical...

As a seasoned Clinical Data Management Specialist, you will be responsible for ensuring the accuracy and quality of clinical trial data. Your expertise in defining project specifications, understanding external data collection, and executing data cleaning strategies will be instrumental in driving success.Key Responsibilities:Data Governance: Develop...

Job Title:Clinical Data Management SpecialistJob Overview:This role involves managing and processing clinical data for trials, ensuring accuracy, quality, and adherence to regulatory standards.Key Responsibilities:Define project specifications for data management services, including protocol conversion, database build, CRF design, and data review and...

Senior Clinical Data Coordinator Job DescriptionOur team seeks an experienced Clinical Data Coordinator to lead project-specific and departmental document tracking activities.Coordinate the development, review, and implementation of data management plans and protocols.Collaborate with cross-functional teams to resolve issues and ensure compliance with...

Clinical Quality Assurance Specialist We are seeking an experienced Clinical Quality Assurance Specialist to provide day-to-day clinical quality assurance (QA) 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...

Job OverviewThe position of Clinical Research Associate is available at our organization. The role involves analyzing and creating clinical trial documents.This job requires the ability to work in a fast-paced environment and maintain compliance with global regulatory standards (FDA, EMA, ICH-GCP). Knowledge of medical terminologies and ontologies is also...

Senior Statistical ProgrammerThe key objective of this position is to provide high-level statistical programming support for multiple clinical projects. The role involves delivering regulatory-compliant output, developing programming documentation, writing efficient code, staying updated on programming techniques, and mentoring staff.Key...

Medical ScribeWe are seeking a skilled Medical Scribe to join our team in this exciting role. The ideal candidate will have 3-5 years of experience as a Live Medical Scriber and possess strong administrative writing skills, reporting skills, and organizational skills.The Medical Scribe will be responsible for reviewing physician dictation and transcribing it...

Lead a Clinical Psychology Service">We are seeking an experienced clinical psychologist to lead our psychology service. As a key member of the team, you will be responsible for developing and implementing treatment plans, supervising junior staff, and ensuring high standards of care.">Key Responsibilities:">">Develop and implement treatment plans that meet...