Senior Clinical Data Specialist

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...

Clinical Data ConfiguratorWe are seeking a highly skilled Clinical Data Configurator to join our team. In this role, you will be responsible for creating and reviewing data specifications, developing analysis datasets, and ensuring compliance with regulatory guidelines.Responsibilities:Create and review data specifications in accordance with industry...

*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...

Sponsor-dedicated roles have become increasingly prominent in the industry.Working fully embedded within a pharmaceutical client, with the support of a global services provider right behind you, you'll be at the heart of their innovation. As a Senior Statistical Programmer you will be dedicated to one of our clients; a company that is driving the next...

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 OverviewA Clinical Data Management Specialist is responsible for defining project specifications, understanding external data collection, and executing data cleaning strategies to ensure high-quality deliverables.Key Responsibilities:Develop project specifications for data management services, including protocol conversion, database build, CRF design,...

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...

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...

Job Title: Clinical Admin Associate">Are you looking for a role that offers stability and growth opportunities? We have an exciting opportunity for a Clinical Admin Associate to join our team.This is a repetitive, SOP-driven back-office role handling templated clinician/clinic communications, records hygiene, and daily logs. No calls. No sales....