- 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
- 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
- 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 work within the Multiple Myeloma clinical research...and ensures study compliance with all state, federal, and IRB requirements. May be responsible for IRB … more
- Beth Israel Lahey Health (Burlington, MA)
- …duties. Implements study protocols in accordance to regulatory and institutional requirements. Works closely with principal investigators, research staff and ... assigned research studies by reviewing study and assessing protocol and institutional requirements: + Implements all study protocols in accordance with research… more
- Dana-Farber Cancer Institute (Brookline, 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 (Boston, MA)
- …samples, maintaining regulatory binders, and ensuring compliance with all institutional , state, and federal regulations, including IRB requirements. ... The Clinical Research Coordinator (CRC) works within the clinical research program...start-up process from receipt of protocols through the Scientific Review Committee and IRB submissions, and site… more
- Boston University (Boston, MA)
- …manuscripts. + Develop IRB protocols and prepare materials for continuing IRB review . Develop organizational tools and protocols. Submit reimbursements from ... **ADMINISTRATIVE RESEARCH COORDINATOR , School of Public Health, Epidemiology** **Job Description** **ADMINISTRATIVE RESEARCH COORDINATOR , School of Public… more
- Dana-Farber Cancer Institute (Milford, MA)
- …site regulatory binders and ensures study compliance with all state, federal, and IRB requirements. May be responsible for site IRB submissions (violations, ... the Regional Campus site(s). + Prepare and/or complete regulatory related reports and IRB submissions as it pertains to the regional campus' studies. Maintain and… more
- Beth Israel Lahey Health (Boston, MA)
- …regulatory support for the projects conducted by the BIDMC Clinical Research Coordinator Core The Clinical Research Coordinator Core provides support for ... (industry, cooperative groups and PI initiated studies), respond to IRB comments on applications submitted and work with study...transfer trials. + Act as a liaison between the IRB and investigator to resolve regulatory queries and concerns.… more
- Beth Israel Lahey Health (Boston, MA)
- …Drug Enforcement Administration. Maintains certification and credentials in accordance with the Board of Registration and adheres to institutional policies and ... is growing our transplant program and seeking a new Clinical Pharmacy Coordinator position with advanced clinical, management and leadership training and experiences… more