The Senior Clinical Research Coordinator (CRC) is responsible for managing and overseeing the day-to-day operations of clinical trials, recruiting and screening study participants, as well as documentin. ...
Under the general supervision of the Senior Clinical Research Program Manager (SCRPM) and the Director of the Center for Vascular Emergencies (CVE), the Clinical Research Coordinator (CRC) provides support for CVE research projects in the Department of Emergency Medicine. MGH Emergency Medicine Clin...
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...
Clinical Research Coordinator I, 20 hrs-(3302635). Working under the supervision of the Administrative Director of Research, Vice Chair and Principal Investigator, and following established policies and procedures, aids on clinical research studies within the Department of Urology. Aids on clinical ...
This position will assist the Principal Investigator (PI) in planning and implementing clinical research studies as assigned. CITI Human Research Protection certification. Monitors the occurrence of clinical adverse events, reporting any to the (PI), the study sponsor and Institutional Review Board....
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 Gastrointestinal (GI) Oncology Clinical Research Program at Dana-Farb...
The Massachusetts General Hospital Center for Aging and Serious Illness (CASI) is seeking Clinical Research Coordinators to support ongoing clinical research focused on patient-centered and caregiver outcomes and improving the lives of older adults and those with serious illness and their care partn...
The Clinical Research Coordinator work within the Center of Cancer Therapeutic Innovation (CCTI) 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 responsibl...
Clinical Research Coordinator serves as a lead team member, subject matter expert and trial coordinator. Senior Clinical Research Coordinator-(3289635). This includes acting as a liaison between the Principal Investigator, clinical collaborators, the study sponsor, clinical trial regulatory groups (...
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 ...
Working under the supervision of the Senior Program Manager and Principal Investigator, the Clinical Research Coordinator will be expected to follow established policies and procedures and provide assistance on clinical research studies. Clinical Research Coordinator I Psychiatry-(3294948). Katherin...
Supervisory duties including overseeing the progress of protocols; supervising, planning and prioritizing the work of the Clinical Research Coordinators. Participates in hiring and training Clinical Research Coordinators. Verifies information with clinical research nurse and/or principal investigato...
The Clinical Research Coordinator will work within the Solid Tumor Biology group and will support the research team in the overall conduct of specimen-based clinical research studies using Good Clinical Practice under the auspices of the Principal Investigator(s) and DFCI Pediatric oncology clinical...
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 ...
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. Responsible for screening research subjects for participation in clinical research projects, enrolling resear...
Includes Clinical roles focused on research projects. Positions in this family perform basic, translational, and/or clinical research towards solving a specific problem for an entity or community. Principal Investigator (PI) in planning and implementing clinical research studies as assigned. This ro...
The Senior Clinical Research Coordinator (CRC) is responsible for managing and overseeing the day-to-day operations of clinical trials, recruiting and screening study participants, as well as documenting and reporting on the daily operations of assigned trials. CRC applies critical thinking and crea...
The Cancer Center Protocol Office is a centralized clinical research office that supports clinical researchers in all disciplines within the Cancer Center. The Clinical Research Coordinator I (CRC I) works under general supervision to support the team in enrolling eligible patients on oncology clini...
Entering data into sponsor EDC and query resolution as the sole Senior Clinical Research Coordinator (SCRC) on-site, the chosen candidate must be adept at protocol comprehension and be capable of working autonomously. Demonstrated ability to work independently, make informed decisions, and drive cli...
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. Current educational initiatives in...
The Senior Clinical Research Coordinator (CRC) is responsible for managing and overseeing the day-to-day operations of clinical trials, recruiting and screening study participants, as well as documenting and reporting on the daily operations of assigned trials. Senior Clinical Research Coordinator. ...
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...
Clinical Research Coordinator I. Performs routine laboratory and clinical procedures (including measuring blood pressure, height and weight, administering cognitive function tests). ...
Duration: 12 Months contract, Full-Time Job Description:The Senior Clinical Research Coordinator (CRC) is responsible for managing and overseeing the day-to-day operations of clinical trials, recruiting and screening study participants, as well as documenting and reporting on the daily operations of...