Intern Clinical Trial Assistant

Assist in preparing, maintaining, and updating the Trial Master File (TMF/eTMF).Support with preparation, submission, and tracking of regulatory and ethics committee documents.Ensure proper filing, version control, and archival of essential study documents.Assist Project Managers and CRAs with study setup, feasibility, initiation, monitoring, and close-out...

Clinical Site Auditor RoleThis position involves guaranteeing adherence to standards and excellence at Clinical Trial sites.Key Responsibilities:Conduct audits of clinical research sites across phases I–IVReview CRFs, informed consent forms, and regulatory documentsIdentify and report audit findings; recommend corrective actionsSupport site staff with...

Senior Technical LeadThe role of a Senior Technical Lead involves providing strategic direction and technical expertise to ensure the successful delivery of clinical trials projects.Develop, validate and maintain SDTM/ADaM datasets, TLFs (Tables, Listings & Figures) and submission-ready outputs in compliance with CDISC standards and regulatory...

Role Overview:We are seeking a talented statistical programmer to join our team. As a statistical programmer, you will play a key role in the development and maintenance of ADaM datasets, TLFs, and other analytical outputs for clinical trials.Your primary responsibilities will include developing, validating, and maintaining ADaM datasets, TLFs, and other...

Job TitleWe are seeking an accomplished Veeva EDC Developer to spearhead the creation of eCRF specifications and design/develop clinical trial setup processes.Collaborate with teams to establish technology standards and governance models.Develop, implement and troubleshoot database setup as per study needs.The ideal candidate will have a strong understanding...

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities...

Job DescriptionLead Statistician for Oncology Clinical TrialsAs a Senior Technical Lead, you will play a critical role in the development and maintenance of SDTM/ADaM datasets, TLFs (Tables, Listings & Figures) and submission-ready outputs. You will be responsible for end-to-end statistical programming activities across all phases of Oncology clinical...

Allahabad India Part time Home-based R1516646Job available in additional locationsClinical Specialist Consultant - Punjabi Speaking Location Remote Virtual Hours Estimated 10-16 hours per month Role Clinical SpecialistAbout IQVIA IQVIA is a global leader in advanced analytics technology solutions and clinical research services dedicated to driving healthcare...

Ambala India Part time Home-based R1516646Job available in additional locationsClinical Specialist Consultant - Punjabi Speaking Location Remote Virtual Hours Estimated 10-16 hours per month Role Clinical SpecialistAbout IQVIA IQVIA is a global leader in advanced analytics technology solutions and clinical research services dedicated to driving healthcare...

Medical Oversight - Provide ongoing medical monitoring of assigned clinical trials, including real-time safety review of adverse events (AEs) and serious adverse events (SAEs). - Evaluate safety signals, trends, and laboratory/ECG abnormalities to ensure participant well-being. - Assess investigator-reported causality and provide independent medical judgment...