Clinical Data Manager

Job Title:Senior Clinical Data CoordinatorAbout This Role:This role involves project-specific and departmental document tracking and control activities, ensuring seamless collaboration among stakeholders. You will review CRF (as per protocol) and project-specific documents, initiate project-specific DMTMF (Data Management Trial Master File) and e-filing, and...

Senior Statistical ProgrammerSponsor-dedicated:You'll be at the heart of a global pharmaceutical company's innovation, driving the next generation of patient treatment where individuals are empowered to work with autonomy and ownership. This is an exciting time to be part of this new program.Position Overview:Leverage your advanced SAS programming skills and...

Job SummaryWe are seeking a highly skilled Clinical Data Analyst to join our team. In this role, you will be responsible for creating and reviewing data specifications, developing analysis datasets, tables, listings, and figures.You will also ensure compliance with ICH-GCP guidelines and core operating procedures.About the RoleThis is an exciting opportunity...

Job SummaryThis role involves overseeing global unblinded CRA teams and providing technical support for unblinded clinical operations.The successful candidate will be accountable for meeting projects' recruitment targets, contributing to the development of project risk mitigation plans, and ensuring clinical quality delivery.Additionally, they will manage...

Job TitleSenior Clinical Research ManagerJob Summary:The Senior Manager of Clinical Research oversees the execution and management of clinical trials and research studies. This involves ensuring projects are completed on time, within budget, and in compliance with regulatory standards.Key Responsibilities:Plan, initiate, and manage clinical research projects...

Senior Clinical Data Manager RoleThis position leads clinical trial data management and data operations teams, ensuring compliance with regulatory requirements.Key Responsibilities:Configure and administer CTMS systems, including CRIO and Veeva Vault CTMS.Develop expertise in EDC platforms and system integrations.Stay up-to-date on regulatory requirements,...

Job Opportunity:Project Leadership PositionThis position involves leading end-to-end clinical reporting projects with a focus on timely and high-quality delivery.Key ResponsibilitiesDevelop, implement and manage clinical reporting projects using R programming language.Design, develop and maintain Shiny dashboards, internal tools and reusable...

Job Summary:We are seeking a Clinical Operations Expert to oversee global clinical teams and provide technical support for clinical operations.Develop and implement strategies to meet recruitment targets.Collaborate with the team to create a project risk mitigation plan and manage clinical risks throughout the project lifecycle.Identify quality standards,...

Clinical Quality Assurance Compliance SpecialistJob Summary:Assume responsibility for overseeing end-to-end clinical trial activities from a quality perspective.Accountable for ensuring Quality Compliance of Clinical Trial Medical Science, Operations, Clinical Trial Supply Management, and Clinical Data Management teams.Review study-related activities,...

**Job Title:** Clinical Quality Assurance SpecialistWe are seeking an experienced Clinical Quality Assurance Specialist to provide day-to-day support across ongoing clinical trials. This individual will play a key role in guiding study teams, maintaining compliance with Good Clinical Practice (GCP), and ensuring quality oversight.Key Responsibilities:Serve...