Senior Clinical Documentation Specialist

About Us:We are a global digital engineering and IT services company that specializes in modernizing technology infrastructure, adopting cloud and AI solutions, and accelerating innovation.Our team operates in over 50 locations across more than 25 countries, with delivery centers in Asia, Europe, and North America.Job Title: Clinical Research AssociateKey...

Clinical Data SpecialistWe are seeking a skilled Clinical Data Specialist to join our team.Job Description:The successful candidate will be responsible for performing User Acceptance Testing (UAT) for CRF screens, database edit checks, and exception reports/listings. They will also test clinical study setup configurations including protocol parameters, visit...

Job Overview: Senior Clinical Quality Assurance ManagerThe role involves overseeing end-to-end clinical trial activities from a quality perspective, ensuring adherence to regulatory requirements and guidelines.This position is responsible for developing and implementing a risk-based approach to quality compliance, safeguarding participants and data...

Senior Clinical Data Coordinator Job DescriptionAs a Senior Clinical Data Coordinator, you will play a pivotal role in ensuring the integrity and accuracy of clinical data. Your responsibilities will include:Key ResponsibilitiesDocument Control: Oversee project-specific and departmental document tracking and control activities to maintain compliance and...

Central Monitoring SpecialistThe Central Monitoring Specialist plays a pivotal role in ensuring the quality and integrity of clinical trial data through centralized monitoring activities, statistical data review, and proactive risk management.Key ResponsibilitiesRisk-Based Quality Management (RBQM) Planning: Lead the development of RBQM plans to ensure the...

*Catalyst Clinical Research*provides customizable solutions to the biopharmaceutical and biotechnology industries through Catalyst Oncology, a full-service oncology CRO, and multi-therapeutic global functional and CRO services through Catalyst Flex. The company's customer-centric flexible service model, innovative technology, expert team members, and...

Job SummaryThe SAS Programmer will be responsible for providing SAS programming support for the Statistics and Data Management functions for all clinical trials and regulatory submissions. The candidate will work closely with Biostatisticians and Data Managers to create SAS programs for independently validating selected tables, listings, and figures and to...

Job Title: Clinical Research AssociateClinical research plays a vital role in medical innovation and drug development. As a key contributor, you will oversee the success of clinical trials.Key Responsibilities:Coordinate trial activities on-site with meticulous supervision.Ensure accurate documentation, site files, and case report forms are...

Clinical Systems Tester RoleWe are seeking a skilled Clinical Systems Tester to join our team in a Decentralized Clinical Trial (DCT) environment. As a key member of our testing team, you will be responsible for testing and validating various digital systems and patient-facing technologies.Author and execute test scripts in Veeva EDC, aligned with protocol...

Job OverviewWe are seeking an accomplished Senior Clinical Data Manager to lead our clinical trial and data management operations. This role requires a minimum of 10-15 years of experience in clinical trials, CTMS platforms, and EDC systems management.Main ResponsibilitiesOversee the implementation of efficient data collection and processing strategies...