- Bausch + Lomb (Boston, MA)
- …(GCP), clinical trials management (including site monitoring), scientific methods, research design, regulatory compliance , and clinical data management. ... established over our 170-year history. We have a significant global research , development, manufacturing and commercial footprint of approximately 13,000 employees… more
- Beth Israel Lahey Health (Boston, MA)
- …with physicians, nurses and fellows. Identifies any problems with protocol compliance and notifies principal investigator and/or research nurse. Begins ... a job, you're making a difference in people's lives.** The Clinical Research Coordinator will support the administration and coordination of the PRECiSE study,… more
- Beth Israel Lahey Health (Boston, MA)
- …with physicians, nurses and fellows. Identifies any problems with protocol compliance and notifies principal investigator and/or research nurse. Begins ... a difference in people's lives.** CORTEX is an expanding collaborative clinical research team focused on developing therapies in neurological diseases. Using a team… more
- Boston College (Chestnut Hill, MA)
- …This position is responsible for management of the University's high-performance research computing functions. This position provides infrastructure support for the ... provide consultation and support to Boston College faculty and principal investigators' research computing project needs. Provides faculty and their research … more
- Beth Israel Lahey Health (Boston, MA)
- …with physicians, nurses and fellows. Identifies any problems with protocol compliance and notifies principal investigator and/or research nurse. Begins ... Drug Development through Phase 1 clinical trials. We conduct cutting-edge research with novel anti-cancer drugs including immunotherapies and targeted drugs, with… more
- Parexel (Newton, MA)
- …or international airport due to travel obligations. Job Title: Senior Clinical Research Associate **Duties:** Parexel International LLC seeks a Senior Clinical ... Research Associate based in Newton, MA to monitor and...visit reports. Develop strategy to configure, distribute, and collect, review , and approve high-quality country-specific and site-specific documents, essential… 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 ... Office to complete the regulatory requirements of the GYN Oncology clinical research project. The RC coordinates aspects of protocol submissions, prepares and… 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 ... research setting - wet lab and/or clinical; familiarity with clinical research protocols, regulatory documents, and IRB procedures; exceptional organizational… more
- Dana-Farber Cancer Institute (Brookline, MA)
- …I, Pre-award position also collaborates with internal stakeholders to address compliance requirements, resolve grievances, and support DFCI's research mission. ... resourcefulness and technological savvy. Comprehensive understanding of proposal development, research administration, and IRB , including knowledge of OMB… more
- ICON Clinical Research (Boston, MA)
- …you will be joining the world's largest & most comprehensive clinical research organisation, powered by healthcare intelligence. Roles and Responsibilities: + Acts ... and activate the site in the shortest possible + Ensure site compliance with study protocol, ICH-GCP, and local/country regulations. + Ensure ongoing adequacy… more