Clinical Research Associate Specialist

We are seeking a Senior Clinical Research Associate to manage, deliver and/or perform full clinical site monitoring services for one or more projects.Key Responsibilities:Act as primary liaison between CRAs and project teamParticipate in the development of project plans, protocols, CRFs, communications or other monitoring forms, documents and toolsRepresent...

The Senior Clinical Analyst and Programmer will lead the programming activities for various purposes including different data listings to be used for data review, Safety Review Listings, Centralized Monitoring Listings and Reports. The Senior Clinical Analyst and Programmer will be responsible to gather, understand and analyze the needs reported by the Data...

The Senior Clinical Analyst and Programmer will lead the programming activities for various purposes including different data listings to be used for data review, Safety Review Listings, Centralized Monitoring Listings and Reports. The Senior Clinical Analyst and Programmer will be responsible to gather, understand and analyze the needs reported by the Data...

Clinical Site Monitoring SpecialistEmbark on a career-enhancing opportunity as a Clinical Site Monitoring Specialist. This role involves developing expertise in site management, data review, and monitoring activities.Key Responsibilities:Drive investigative site recruitment, compliance, and oversight through effective site management practices.Conduct remote...

The Regulatory Affairs Associate will support the preparation, tracking, and coordination of Ethics Committee (EC) and Regulatory Authority (RA) submissions. Under supervision, the Associate will assist the Regulatory Affairs team in ensuring that clinical trial submissions comply with applicable regulations and internal timelines.More specifically, the...

We are seeking a Clinical Data Specialist to join our team. The successful candidate will be responsible for providing support to activities related to coding of clinical data for ongoing clinical studies.The ideal candidate will have thorough knowledge of medical terminology and experience working with clinical trials or within the pharmaceutical...

The Regulatory Affairs Associate will support the preparation, tracking, and coordination of Ethics Committee (EC) and Regulatory Authority (RA) submissions. Under supervision, the Associate will assist the Regulatory Affairs team in ensuring that clinical trial submissions comply with applicable regulations and internal timelines. More specifically, the...

Manage, deliver and/or perform full clinical site monitoring services for one or more projects, which may include multiple services, be complex in nature and/or run on a multinational scale. In-house based position, responsible for the design and oversight of project monitoring services including training, site/patient recruitment, site data/document...

Manage, deliver and/or perform full clinical site monitoring services for one or more projects, which may include multiple services, be complex in nature and/or run on a multinational scale. In-house based position, responsible for the design and oversight of project monitoring services including training, site/patient recruitment, site data/document...

Job Title: Vendor Manager">">The Vendor Manager is a key member of our team, responsible for establishing and managing project supplier and vendor scope, timelines, and costs throughout the project life cycle.">He/She will ensure ongoing operational and financial oversight, and risk and issue management of vendors.">This role requires close collaboration...