Clinical Research Associate Specialist

Job Description:">The Site Selection Specialist is a vital member of the project team, serving as the primary point of contact for site selection activities. This includes identifying and evaluating potential research sites to ensure they meet specific criteria.">This role is perfect for those with experience working in clinical research, particularly in...

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...

Clinical Research Manager Job DescriptionWe are seeking a highly skilled Clinical Research Manager to oversee the planning, execution, and completion of clinical research projects. This is a challenging opportunity for a results-driven individual to utilize their project management expertise in a dynamic environment.Job Responsibilities:Manage...

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...

Join us in redefining what it means to work for a CRO. When you work at Rho, it’s more than just a job—you become part of the Rho Factor. We’re a proud bunch of science nerds who love tackling big challenges together. We’re not your typical CRO, and we’re not trying to be. Here, curiosity is encouraged, fresh approaches are welcome, and...

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...