Knowledge of Good Clinical Data Management Practices, CDASH/CDISC, SDTM, Medical Terminology, GCP, ICH Guidelines, and 21 CFR Part11 Knowledge of SAS. Knowledge of paper, EDC, and hybrid-base data collection and processing.
A medical devices company is filling a position for a Telecommute Lead Clinical Research Associate. Core Responsibilities Include: Participating in multiple internal cross functional teams. Participating in project team meetings. Electing qualified and experienced research sites.
Qualifications Include: MA or MS in statistics subject, preferably with a strong medical statistics component. 8 years of postgraduate experience in the application of statistics to clinical trials for employees with an MA/MS in statistics subject.
A pharmaceuticals is in need of a Remote Medical Monitor. Core Responsibilities Include: Working with the clinical team to review the safety data using different tools. Monitoring and cleaning ongoing oncology studies, and support database locks.
A biopharmaceutical organization has an open position for a Telecommute Senior Medical Regulatory Writer. Individual must be able to fulfill the following responsibilities: Compiling, writing, and editing medical writing deliverables. Serving as a medical writer on project teams.
A contract research organization is in need of a Telecommute Oncology Senior Medical Director. Individual must be able to fulfill the following responsibilities: Provide continuous medical monitoring during study conduct, answers site questions on inclusion/exclusion criteria.
A full-service contract research organization has a current position open for a Telecommute Medical Monitoring Associate in Nashville. Individual must be able to fulfill the following responsibilities: Providing support to site staff.
Reviewing medical files and providing recommendations. Skills and Requirements Include: Attends orientation and training. Must be in active medical practice to perform appeals. Board certified MD, DO, Current, unrestricted clinical license. Post-graduate experience in direct patient care.
Minimum 5 years monitoring experience in a pharmaceutical or medical device company or CRO. Advanced skills in Microsoft Word, Microsoft PowerPoint, Microsoft Excel, Microsoft Outlook. Strong knowledge, understanding, and application of monitoring SOPs and Good Clinical Practice.
A medical company needs applicants for an opening for a Telecommute Senior Oncology Project Manager. Core Responsibilities of this position include: Preparing and actively participating as operational lead in internal project review meetings.