The Clinical Research Coordinator is an entry human subjects researcher, responsible for conducting and assisting in clinical research studies under the supervision of the Principal Investigator or se...

The Clinical Research Coordinator is an entry human subjects researcher, responsible for conducting and assisting in clinical research studies under the supervision of the Principal Investigator or se...

The Clinical Research Coordinator is an entry human subjects researcher, responsible for conducting and assisting in clinical research studies under the supervision of the Principal Investigator or se...

Internally, we call them CISs (Clinic Informatics Specialists) in recognition of their important role in supporting accurate, specific, and timely clinical documentation. This is an excellent opportun...

Clinical Research Coordinator analyzes and interprets highly complex clinical research data; conducts clinical testing and develops protocols. Analyzes highly complex data gathered on clinical researc...

Internally, we call them CISs (Clinic Informatics Specialists) in recognition of their important role in supporting accurate, specific, and timely clinical documentation. This is an excellent opportun...

The Clinical Research Coordinator (CRC) is an entry human subjects researcher, responsible for assisting the lab leadership (including but not limited to CRC I), in clinical research studies. Conducts...

Under general direction, the Clinical Research Specialist is responsible for the administration, execution, and overall management of clinical research studies. Society of Clinical Research Associates...

Under general direction, the Clinical Research Specialist is responsible for the administration, execution, and overall management of clinical research studies. Society of Clinical Research Associates...

The Clinical Research Coordinator's primary responsibilities are to utilize Good Clinical Practices (GCP)s in the process of screening, enrolling and closely monitoring clinical research study subject...

Internally, we call them CISs (Clinic Informatics Specialists) in recognition of their important role in supporting accurate, specific, and timely clinical documentation. This is an excellent opportun...

Company history: Brooklyn Clinical Research was founded to increase access to clinical trials for underrepresented populations. This range is provided by Brooklyn Clinical Research. Clinical research ...

Company history: Brooklyn Clinical Research was founded to increase access to clinical trials for underrepresented populations. This range is provided by Brooklyn Clinical Research. Clinical research ...

Title: Clinical Research Coordinator. The successful candidate will be responsible for assisting with various clinical research activities, including statistical analysis, literature reviews, manuscri...

Minimum 5 Years of experience required in Research Nursing or other relevant area. Responsible for coordinating and performing study specific clinical activities across multiple study protocols of dif...

Minimum 5 Years of experience required in Research Nursing or other relevant area. Responsible for coordinating and performing study specific clinical activities across multiple study protocols of dif...

Company history: Brooklyn Clinical Research was founded to increase access to clinical trials for underrepresented populations. To support this objective, we establish clinical research sites in dense...

Company history: Brooklyn Clinical Research was founded to increase access to clinical trials for underrepresented populations. Clinical research experience is a plus but not required. To support this...

Title: Clinical Research Coordinator. The successful candidate will be responsible for assisting with various clinical research activities, including statistical analysis, literature reviews, manuscri...

Title: Clinical Research Coordinator. The successful candidate will be responsible for assisting with various clinical research activities, including statistical analysis, literature reviews, manuscri...

Collect and manage clinical trial data from different sources, like forms and electronic systems. Check for errors or mismatches in the data and work with the research team to fix them. Review data to...

Collect and manage clinical trial data from different sources, like forms and electronic systems. Check for errors or mismatches in the data and work with the research team to fix them. Review data to...

Trains clinical staff on study protocols and procedures and supervises the Clinical Research Unit (CRU) staff when the principal investigator or sub-investigators are not present to direct clinical re...

Experience in clinical research, clinical trials, or a medical-related profession is highly preferred. Coordinate team members to complete clinical and non-clinical assessments per protocol, including...

Experience in clinical research, clinical trials, or a medical-related profession is highly preferred. Coordinate team members to complete clinical and non-clinical assessments per protocol, including...

The Clinical Research Coordinator’s primary responsibilities are to utilize Good Clinical Practices (GCPs) in the process of screening, enrolling and closely monitoring clinical research study subject...

The Clinical Research Coordinator’s primary responsibilities are to utilize Good Clinical Practices (GCPs) in the process of screening, enrolling and closely monitoring clinical research study subject...

The Coordinator drives recruitment and assists research participants on clinical research studies, coordinates and schedules participant clinic visits, and serves as principal administrative liaison f...

The Coordinator drives recruitment and assists research participants on clinical research studies, coordinates and schedules participant clinic visits, and serves as principal administrative liaison f...

Reporting to the Senior Scientist at and working in collaboration with the SFARI Data & Biospecimens Repository (SDBR) and Informatics Teams, the Clinical Research Specialist will support various data...

Reporting to the Senior Scientist at and working in collaboration with the SFARI Data & Biospecimens Repository (SDBR) and Informatics Teams, the Clinical Research Specialist will support various data...

Provides informatics analysis and support in the use of clinical information systems as assigned. Participates in the formulation of new or revised policies and procedures related to the clinical appl...

Provides informatics analysis and support in the use of clinical information systems as assigned. Participates in interdisciplinary and process improvement teams to identify potential enhancements of ...

Nursing Institute, Institute for Clinical Excellence, Medication Safety committee, Evidence-Based Research committee, etc. Collaborates with management and clinicians in designing, implementing and ma...

Nursing Institute, Institute for Clinical Excellence, Medication Safety committee, Evidence-Based Research committee, etc. Supports clinical staff in the real time application of information to change...

Oversees and resolves operational aspects of clinical trials in conjunction with project teams and in accordance with standard operating procedures (SOP), good clinical practice (GCP) and specific cou...

Oversees and resolves operational aspects of clinical trials in conjunction with project teams and in accordance with standard operating procedures (SOP), good clinical practice (GCP) and specific cou...

Position Summary Working in the Division of General Medicine under the direction of the Principal Investigator, the Coordinator will provide coordination and data collection in NIH-sponsored research ...

The Clinical Research Specialist serves as a regulatory expert and resource for investigators and others within the Clinical Research Support Office in the Hospital. The Clinical Research Specialist c...

The Clinical Research Specialist serves as a regulatory expert and resource for investigators and others within the Clinical Research Support Office in the Hospital. The Clinical Research Specialist c...