- Norstella (Boston, MA)
- …our solutions. + Ensure all work complies with relevant regulatory requirements (eg, IRB , EC, GCP) and data privacy standards. + Mentor junior project managers and ... of clinical trial operations, patient recruitment strategies, regulatory requirements ( IRB /EC), and GCP standards. + Proficiency in project management tools… more
- Beth Israel Lahey Health (Boston, MA)
- …submit applications (industry, cooperative groups and PI initiated studies), respond to IRB comments on applications submitted and work with study team in getting ... on oncology human gene transfer trials. + Act as a liaison between the IRB and investigator to resolve regulatory queries and concerns. + Assist in the preparation… more
- Boston University (Boston, MA)
- …manuscripts. + Develop IRB protocols and prepare materials for continuing IRB review . Develop organizational tools and protocols. Submit reimbursements from ... conferences and research meetings. **Required Skills** Required skills: + A master's degree in a related discipline is required. + 1-3 years of experience. + Excellent oral, written, and interpersonal communication skills. + Demonstrated experience working in… more
- Massachusetts Institute of Technology (Cambridge, MA)
- …projects; identify and resolve bottlenecks or delays; ensure adherence to IRB protocols, sponsor timelines, and regulatory compliance; maintain documentation of ... clinical; familiarity with clinical research protocols, regulatory documents, and IRB procedures; exceptional organizational and communication skills; strong problem-solving… more
- Beth Israel Lahey Health (Boston, MA)
- …visits for subjects. (essential) 7. Assists investigator with correspondence with IRB . (essential) 8. As needed, may function in areas/clinics performing job ... duties related to clinical research studies. **Required Qualifications:** + Bachelor's degree required. + 0-1 year of related work experience required. + Medical terminology. + Working knowledge of computer systems required, including web-based applications… more
- Tufts Medicine (Boston, MA)
- …We have two full-time Neurology clinical research coordinators that help with IRB , trial, and registry support. **Education** **:** Our faculty are full-time ... participate in research, provide didactics to trainees, develop and modify institutional guidelines and policies, and participate in hospital-wide committees. **Work… more
- Dana-Farber Cancer Institute (Boston, MA)
- …Specialist will be responsible for the collection, management, and quality assurance review of patient clinical data. Located in Boston and the surrounding ... tracking systems (STIP) and laboratory binders. + May be responsible for IRB and regulatory submissions and maintenance of regulatory files. **For Bone Marrow… more
- Massachusetts Institute of Technology (Cambridge, MA)
- …research sites, and contribute to technical sections of project reports and IRB applications; and may include mentoring student interns, onboarding new team members, ... and assisting with literature reviews and academic writing. Job Requirements REQUIRED: Bachelor's degree with strong economics and quantitative coursework; experience handling large datasets; proficiency in relevant statistical software; excellent written and… more
- Dana-Farber Cancer Institute (Boston, MA)
- …Data Specialist will be responsible for the collection, management, and quality assurance review of patient clinical data. The Research Data Specialist will play a ... tracking systems (STIP) and laboratory binders. + May be responsible for IRB and regulatory submissions and maintenance of regulatory files. + Bachelor's Degree… more
- Dana-Farber Cancer Institute (Brookline, MA)
- …Specialist will be responsible for the collection, management, and quality assurance review of patient clinical data. There is no responsibility to consent eligible ... tracking systems (STIP) and laboratory binders. + May be responsible for IRB and regulatory submissions and maintenance of regulatory files. + Bachelor's Degree… more