Trial Master File Specialist

Job DescriptionJob Title: Consultant Clinical Trials, Global Regulatory Application Specialist for AI ApplicationLocation: Pune (Remote / Flexible)About UsDizzaroo Private Limited is developing an AI-powered application to streamline and accelerate the global clinical trial application process. Our platform is designed to simplify the preparation,...

Job OverviewThe Senior Clinical Systems Specialist oversees the effective execution of clinical trials and programs. This role requires an individual with extensive experience in eClinical systems, particularly in maintaining the quality of the Trial Master File (TMF).Key ResponsibilitiesConduct TMF quality reviews to ensure accuracy and completeness of...

Senior Biostatistician RoleThe Senior Biostatistician drives success in clinical trials through strategic statistical leadership. This pivotal role spearheads planning, execution, and interpretation of statistical analyses across development programs.Key Responsibilities:Lead biostatistics for assigned studies and projects, ensuring timely execution of...

Job SummaryWe are seeking a motivated and detail-oriented Clinical Trials Specialist to join our team. In this role, you will be responsible for managing and reviewing adverse events, product quality complaints, and medical information.Key ResponsibilitiesManage and review expeditable adverse events, product quality complaints, and medical information.Submit...

Job DescriptionThe Specialist shall be responsible for processing information, ensuring data integrity and quality. This role requires attention to detail, efficiency, and the ability to work collaboratively within a team.Core activities include processing Indian Custom filings on behalf of clients, which involves meticulous attention to detail, data...

Job Description- Review and manage Trial Master Files (TMF) to ensure completeness and compliance.- Organize and maintain TMF documents.- Conduct regular audits of TMF to identify and resolve discrepancies.- Collaborate with clinical teams to ensure timely and accurate documentation.- Provide training and support on TMF best practices.

Job Overview:The role of a Clinical Study Researcher and Medical Writer is multifaceted, requiring expertise in clinical trial documentation, scientific communication, and regulatory compliance.Key Responsibilities:Develop high-quality key clinical trial documents, including protocols, Investigator's Brochures (IBs), Informed Consent Forms (ICFs), Case...

Systems Plus is hiring for LIMS Master Data Specialist Exp : 3 yr +Location : Pune Magarpatta.Hybrid.Work timing : 2 to 10 pm IST.JD : What You'll Do As a LIMS Master Data Specialist, you will:• Review source documentation for master data objects such as laboratory methods and analysis• Create/ build master data objects in the LIMS, including test...

MDM Technical ConsultantWe are seeking a highly skilled MDM Technical Consultant to join our team. As an MDM Technical Consultant, you will be responsible for designing and developing technical architecture for Master Data Management (MDM) systems.The ideal candidate will have excellent knowledge of Oracle MDM Technical - Application Composer, Page Composer,...

SystemsPlus is hiring for LIMS Master Data Specialist Exp : 3 yr + Location : Pune Magarpatta. Hybrid. Work timing : 2 to 10 pm IST. JD : What You'll Do As a LIMS Master Data Specialist, you will: • Review source documentation for master data objects such as laboratory methods and analysis • Create/ build master data objects in the LIMS, including test...