Under the general direction of the Principal Investigator (PI) or designee, the Clinical Research Coordinator III is responsible for independently performing delegated tasks and procedures involving human subject research. Clinical Research Coordinator III. Responsible for clinical research billing ...
Under the direction of the Principal Investigator (PI) or designee, the Clinical Research Coordinator II is responsible for independently performing delegated tasks and procedures involving human subject research. Clinical Research Coordinator II. May be responsible for clinical research billing rev...
Develop SEAS specific clinical research and IRB procedures in collaboration with SEAS Science Operations to support IRB research at our numerous research sites. Engage with the SEAS clinical research team and faculty in developing best practices and protocol restructuring proactively. This position ...
New graduates with some relevant course/project work or those without any prior research experience will be considered for the Clinical Research Coordinator I position outlined above. Clinical Research Coordinator-(3294569). Those with a minimum of 1-2 years of directly related work experience will ...
Minimum of three years in a Clinical Research Coordinator role. This is a contract position and requires previous Ophthalmology clinical research experience*. ...
Under the direction of the Director of Operations and Clinical Research Project Manager, the Clinical Research Coordinator will work independently on ongoing research studies. A Clinical Research Coordinator II performs the duties of a Clinical Research Coordinator I (above) and may also:. Clinical ...
The Clinical Research Coordinator work within the clinical research program and support the research team in the overall conduct of clinical trials using Good Clinical Practice under the auspices of the Principal Investigator. The CRC will be responsible for the primary data collection and managemen...
The Clinical Research Coordinator work within the Cantor Center clinical research program and support the research team in the overall conduct of clinical trials using Good Clinical Practice under the auspices of the Principal Investigator. The CRC will be responsible for the primary data collection...
Bachelors degree and 1 year of experience in a medical setting and/or clinical research preferred. Day (United States of America)Job Summary: Responsible for screening patients for participation in clinical trials, enrolling patients onto these studies, monitoring protocol implementation, completing...
A Clinical Research Coordinator II performs the duties of a Clinical Research Coordinator I (above) and may also:. New graduates with some relevant course/project work or those without any prior research experience will be considered for the Clinical Research Coordinator I position outlined above. C...
We are seeking a highly motivated Clinical Research Coordinator II to support our clinical trials research studies. Clinical Research Coordinator II, Dept of Dermatology-(3298026). The Clinical Research Coordinator II will be responsible for the following activities:. Experience in clinical research...
Participating in clinical and research meetings to assist the Head and Neck Team in conducting research studies and clinical trials. Research coordinators are invited to attend journal clubs, monthly research meetings, weekly clinical trial meeting, weekly tumor board and sample collection meetings....
Clinical Research Coordinator serves as a lead team member, subject matter expert and trial coordinator. Senior Clinical Research Coordinator-(3298531). This includes acting as a liaison between the Principal Investigator, clinical collaborators, the study sponsor, clinical trial regulatory groups (...
The Clinical Research Coordinator will welcome families, inform them about the research study, obtain consent, and administer/score a range of assessments designed to characterize study participants. Clinical Research Coordinator I-(3303889). The Clinical Research Coordinator I (full-time) will join...
The Clinical Research Coordinator will report to the Project Manager and will work closely with biostatisticians, data managers, and study staff to support study operations, data collection and quality control, and reporting of research findings. Day JobPosted Shift Description:We are looking for a ...
Regularly interfaces with current and potential clinical trial participants to determine eligibility and consent of study participants in alignment with clinical trial protocol. Perform clinical duties: vitals, phlebotomy, EKGs, and other patient care skills. Communicates and collaborates specific s...
The Clinical Research Coordinator work within the Genitourinary (GU) Oncology clinical research program and support the research team in the overall conduct of clinical trials using Good Clinical Practice under the auspices of the Principal Investigator. Qualifications Bachelor’s Degree or 1 year of...
Headquartered in Birmingham, No Resistance is a clinical trial site management organization that performs clinical trials in urgent care centers throughout the north and southeast. No Resistance is seeking motivated individuals to join our team! In this role, you'll play a pivotal part in the implem...
The Clinical Research Coordinator (CRC) will work within the Multiple Myeloma clinical research program and support the research team in the overall conduct of clinical trials using Good Clinical Practice under the auspices of the Principal Investigator. The CRC will be responsible for the primary d...
The Clinical Research Coordinator work within the Center of Cancer Therapeutic Innovation clinical research program and support the research team in the overall conduct of clinical trials using Good Clinical Practice under the auspices of the Principal Investigator. The CRC will be responsible for t...
Bachelors degree and 1 year of experience in a medical setting and/or clinical research preferred. Day (United States of America)Job Summary: Responsible for screening patients for participation in clinical trials, enrolling patients onto these studies, monitoring protocol implementation, completing...
The Regulatory Coordinator will contribute to the regulatory/ethics/IRB submission consultations process, ongoing educational initiatives, and Research Professionals Network (RPN) of the Clinical Research Resources Office (CRRO) at Boston University Medical Campus. REGULATORY COORDINATOR, School of ...
Independently or in conjunction with other clinical research staff and/or research nurse, recruits and enrolls research subjects onto clinical research projects according to study protocols. Verifies information with clinical research nurse and/or principal investigator. Responsible for screening pa...
Must be flexible as hours may change for events.POSITION SUMMARY (Limit to a few sentences to explain the main purpose of the role).This role will under general direction of the department management, coordinate the data management for the departments.They will maintain the databases using excel for...
These positions work within the clinical research program and support the research team in the overall conduct of clinical trials using Good Clinical Practice under the auspices of the Principal Investigator(s) and the DFCI Clinical Trials Office. The Pediatric Cancer Predisposition program is looki...