Offshore Decentralized Clinical Trials Tester

Job OverviewWe are seeking a skilled Clinical Systems Tester with expertise in Veeva CDMS and hands-on experience with eCOA and IRT platforms.This role supports testing and validation activities within a Decentralized Clinical Trial (DCT) environment, requiring flexibility across various digital systems and patient-facing technologies.

Clinical Research Associate Job DescriptionWe are seeking a highly motivated and organized Clinical Research Associate to join our team.Assist with on-site coordination of clinical trial activities under supervision, ensuring all trial activities adhere to ICH-GCP and ethical guidelines.Maintain essential documents, site files, and case report forms,...

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...

Job Title: Senior Statistical ProgrammerSponsor-dedicated:You'll be embedded within a global pharmaceutical client, working closely with Cytel's support team. This is an exciting time to contribute to their innovation.Position Overview:Leverage your advanced SAS programming skills and CDISC standards proficiency (SDTM & ADaM) to support or lead Phase I-IV...

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....

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 Opportunity:Senior Clinical Data Coordinator">We are seeking a highly skilled Senior Clinical Data Coordinator to join our team. The successful candidate will be responsible for project-specific and departmental document tracking and control activities.Key Responsibilities:The Senior Clinical Data Coordinator will have the following key...

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...

Python Quality Assurance Tester RoleWe are seeking a skilled Quality Assurance Tester to validate API responses using Python. The ideal candidate has a strong understanding of REST APIs, JSON, and XML.Key Responsibilities:Proficiency in Python and automation frameworks such as PyTest.Solid understanding of Agile methodologies and continuous integration...

Job OverviewWe are seeking a highly skilled professional to support the development of an innovative AI digital health and medical device platform. The successful candidate will have a strong background in addiction medicine, substance use disorder treatment, psychosis, and/or pain management.The role requires clinical expertise in patient assessment,...