In this role, you will assist in the development of research study budgets for new clinical trials, and helps ensure that appropriate billing or charging mechanisms are in place for research charges related to the research study.
In this role, the selected candidate will support the goals of the Gen Med organization by initiating, monitoring, and closing out clinical study sites following GCP and ICH guidelines as well as Novartis SOPs and ensuring that study milestones are met.
In this role, you will supports assigned projects by creating and monitoring project budgets, conducting data analysis and implementing process improvement plans to assure timely and successful project completion.
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$60K to $80K -Dallas, TX
In this role, you will assist in implementing University Healthcare Consortium (UHC) benchmarking findings, technology assessments and other UHC initiatives. Provides recommendations to identify specific financial goals and objectives and initiatives to realize Parkland strategic goals.
In this role, the selected candidate serves as a liaison between the Clinical Departments and IT, to ensure clear and effective bi-direction communication related to user needs and system capabilities.
In this vital Registered Nursing role, you will coordinate ESRD patient care and services (trend lab values, track metrics on vital signs, weight, outcome management, etc.); you will ensure you and your clinical team are delivering the highest level of care to our patients by ensuring their safety, comfort, and well being.
The Clinical Research Associate (CRA) position represents an opportunity to grow within an emerging medical device company. Solid knowledge of the processes involved in clinical studies following Good Clinical Practice (GCP/ICH) and the appropriate regulations is required.
The primary function of the Specialty Clinics Bleeding Disorders Nurse is to provide nursing care in the clinical setting and to coordinate the comprehensive and complex care of the Bleeding Disorders population, specifically the hemophilia population.
In this role, you will be a human bridge between research, knowledge management, marketing and communications, with a sustained focus on coordinating research projects and improving our design intelligence as a firm.
In this role, you will be responsible for assisting with the planning and implementation of clinical research studies including oversight of registry, biology and basic treatment trials and also direct supervision of other CRA and subordinate team members.
In this role, the selected candidate will review relevant Standard Operating Procedures (SOPs) and introduce new SOPs as appropriate; participates in client meetings, study initiation visits, and study update meetings as necessary.