Clinical Trials Data Specialist

Statistical ProgrammerWe are seeking a skilled Statistical Programmer to join our team. In this role, you will be responsible for developing and maintaining ADaM datasets and other analytical outputs for clinical trials.Key Responsibilities:Develop, validate, and maintain ADaM datasets, TLFs, and other analytical outputs for clinical trials.Support Oncology...

Clinical Assurance Specialists play a pivotal role in ensuring compliance and quality at clinical trial sites.Responsibilities:Conducting thorough audits of clinical research sites across various phasesReviewing case report forms, informed consent documents, and regulatory materialsIdentifying and reporting audit findings; recommending corrective actions to...

Job OverviewThis Application Support Engineer role requires excellent communication skills and a good understanding of clinical trials domain.The ability to troubleshoot and resolve client-specific technical cases, assist with escalation of cases from level one & two support staff, assist with client projects moving from project to production environment,...

Senior Statistical Programming LeadThis position offers the opportunity to work with our team on end-to-end statistical programming activities, focusing on Oncology clinical trials.We are seeking a highly skilled and experienced Senior Statistical Programming Lead to join our team. The successful candidate will have strong working knowledge of ISS or ISE...

As a Statistical Programmer, you will play a crucial role in programming all tables, listings and graphs necessary for an assigned clinical study report (CSR) using Base SAS programs, SAS procedures, or standardized macros.The role requires analyzing protocol, SAP, existing shells/templates as needed to understand structure and content of data, performing...

Quality Assurance Auditor Job TitleThe position of Clinical Site Auditor entails ensuring compliance and quality at Clinical Trial sites by conducting site audits, reviewing documentation, verifying adherence to protocols, GCP, GLP, and regulatory requirements.Conducting audits of clinical research sites across phases I–IV is a crucial aspect of this...

Job Title: Clinical Affairs & Professional Relationship ExecutiveLocation: Trichy Salary: ₹50,000 per month Total Vacancies: 3 (Preferably Male) Qualification Required: BDS (Bachelor of Dental Surgery) Travel Requirement: Extensive travel across multiple territories in India Travel Benefits: Travel, accommodation, and food will be provided for all...

**Statistical Programmer Role Overview:**We are seeking a highly skilled Statistical Programmer to join our team. The ideal candidate will have expertise in R programming and SAS programming, with a strong focus on ADaM dataset development and TLF programming.This is an exciting opportunity for a motivated individual to work on clinical trials and contribute...

Job OverviewAs a Global Lead Statistical Programmer, you will be responsible for leading and managing statistical programming activities in various studies and projects. This role requires a strong understanding of pharmaceutical clinical development, regulatory submissions, and CDISC standards.The ideal candidate will have excellent SAS programming skills,...

Job Opportunity:Hiring for an AI Scientist to work on a long-term contract basis remotely. The role focuses on leveraging and augmenting existing models to generate insights that support clinical studies and oncology research in the pharma domain.Utilize foundation models for healthcare and pharma-specific datasets, driving data analysis and insight...