- Children's Hospital Boston (Boston, MA)
- …per Week:40 Job Posting Category:ResearchJob Posting Description:Under direct supervision, the IRB Coordinator will coordinate all activities and functions of ... review activities for the BCH human subjects program ( IRB ) to ensure that goals and objectives specified for...team coming in-person a few times a month. This IRB Coordinator will be responsible for: +… more
- Tufts Medicine (Boston, MA)
- …study sponsor and Institutional Review Board . 5. Assists with Institutional Review Board ( IRB ) requirements for each study including meeting ... institutional educational requirements, submitting documents for review such as amendments, adverse event reporting and annual reviews. 6. Performs basic… more
- Caris Life Sciences (Boston, MA)
- …clinical database. + Support and adhere to Good Clinical Practices (GCP) guidelines, FDA, Institutional Review Board ( IRB ) and HIPPA regulations, Site ... **Position Summary** The Clinical Data Coordinator is responsible for clinical data entry activities...outcomes for oncology patients. Responsible for the collection and review of clinical protocol research data; Interpretation of data… more
- Beth Israel Lahey Health (Boston, MA)
- …research nurse, submits protocols, amendments, notices, suspensions and terminations to the IRB for review and approval. (essential) + Interacts with patients ... multiple clinical trials, ensuring compliance with federal, state and institutional guidelines. Financial responsibilities including assisting with the grant… more
- Beth Israel Lahey Health (Burlington, MA)
- …assigned research studies by reviewing study and assessing protocol and institutional requirements: + Immediately develops coordinator /sponsor relationship. + ... clinical trials. Implements study protocols in accordance with regulatory and institutional requirements. Uses administrative systems to manage the progress of each… more
- Dana-Farber Cancer Institute (Boston, MA)
- …the research study start-up process from receipt of protocols through the Scientific Review Committee and IRB submissions, and site activation activities. + ... Cancer Predisposition program is looking for a Clinical Research Coordinator II to join their group to assist in...and ensures study compliance with all state, federal, and IRB requirements. May be responsible for IRB … more
- Spaulding Rehabilitation (Charlestown, MA)
- …clinical science or public health + Prior experience as a clinical research coordinator + Familiarity with IRB policies and procedures Preferred + ... Sr Clinical Research Coordinator - ( 3305453 ) **Description** **Overview:** We...recruitment and data collection activities, preparation and management of IRB actions, data quality assurance, preparation of agendas for… more
- Dana-Farber Cancer Institute (Boston, MA)
- …the clinical trials start-up process from receipt of protocols through the Scientific Review Committee and IRB submissions, and site activation activities. + ... The Clinical Research Coordinator (CRC) will work within the Center of...and ensures study compliance with all state, federal, and IRB requirements. May be responsible for IRB … more
- Dana-Farber Cancer Institute (Boston, MA)
- …the clinical trials start-up process from receipt of protocols through the Scientific Review Committee and IRB submissions, and site activation activities. + ... Therapies and Healthy Living is recruiting a Clinical Research Coordinator I (CRC I). The CRC I is a...and ensures study compliance with all state, federal, and IRB requirements. May be responsible for IRB … more
- Dana-Farber Cancer Institute (Boston, MA)
- …applications, amendments, continuing reviews, and informed consent documents for SRC and IRB review and approval + Prepares and submits regulatory documentation ... coordination of assigned study monitoring and auditing visits with study coordinator , Investigator, DF/HCC QACT, Industry Sponsors, and third party auditors.… more
- Dana-Farber Cancer Institute (Brookline, MA)
- …the clinical trials start-up process from receipt of protocols through the Scientific Review Committee and IRB submissions, and site activation activities. + ... and identifying potential targets for intervention. The Clincal Research Coordinator (CRC) will be responsible for the primary data...and ensures study compliance with all state, federal, and IRB requirements. May be responsible for IRB … more
- Beth Israel Lahey Health (Boston, MA)
- … will report directly to the Director of Clinical Research Operations. The Coordinator will assist with research team education, IRB applications and study ... The Department of Neurology at BIDMC is seeking a Clinical Research Coordinator to support a centralized clinical research program. The Department provides… more
- Spaulding Rehabilitation (Charlestown, MA)
- Clinical Research Coordinator II - ( 3305907 ) **Description** **Overview:** We are recruiting a highly motivated individual with a passion for rehabilitation ... research to serve as a Clinical Research Coordinator II (CRC II) in the Long-term Assessment and...recruitment and data collection activities, preparation and management of IRB actions, data quality assurance, preparation of agendas for… more
- Boston University (Boston, MA)
- The Boston University Amyloidosis Center is seeking a Research Study Coordinator to work on one or more international multi-center clinical trials. The Research ... Study Coordinator will perform research and administrative tasks including but...not limited to responsibility of all financials, oversight of IRB communications, and direct management of subjects in the… more
- Dana-Farber Cancer Institute (Brookline, MA)
- …the clinical trials start-up process from receipt of protocols through the Scientific Review Committee and IRB submissions, and site activation activities. + ... The Senior Clinical Research Coordinator work within the clinical research program and...and sample collection. The CRC may be responsible for IRB protocol submissions (amendments, continuing reviews, SAEs, violations/deviations and… more
- Boston University (Boston, MA)
- …Local Public Health Institute (https://sites.bu.edu/masslocalinstitute/) (LPHI). The Project Coordinator is responsible for subject recruitment, payment, scheduling, ... cleaning of the data and ensuring data integrity. The coordinator will assist the research manager with developing and...will assist the research manager with developing and managing IRB and HRPO application and protocol documents as well… more
- Harvard University (Cambridge, MA)
- …Business Title:Research Assistant IV Lab (Laboratory Coordinator )Sub-Unit: Salary Grade (https://hr.harvard.edu/salary-ranges#ranges) :055Time Status:Full-time ... + This position has a 90 day orientation and review period. The O&R period will be waived for...+ Manages lab operations including maintaining and amending IACUC, IRB and COMS approvals; coordinates access to and training… more
- Beth Israel Lahey Health (Boston, MA)
- …Bowdoin Street Health Center and is part of the BIDMC Clinical Research Coordinator Core. The coordinator will be responsible for screening research subjects ... responsibilities include coordinating operations with the main BIDMC Clinical Research Coordinator core. The candidate must have familiarity with the patient… more
- Tufts Medicine (Boston, MA)
- …and practices related to job area. **Job Overview** The Research Project Coordinator serves as the link between administrative staff, fellows and faculty, and ... through maintaining social outlets. 5. Organizes and maintains the list of active IRB protocols to better understand the landscape of research, find better ways to… more
- Boston University (Boston, MA)
- The Human Research Education & QA Coordinator will contribute to the regulatory/ethics/ IRB submission consultations process, ongoing educational initiatives, and ... Workshops, and Summer Sessions. The Human Research Education & QA Coordinator will perform responsibilities related to educational offerings including scheduling,… more