- Merck (Boston, MA)
- …portfolio and compliance with public disclosure of clinical trials and their results. The Senior Informed Consent Medical Writer is responsible for ... regulatory requirements, and health literacy principles. **With minimal oversight, the Senior Informed Consent Medical Writer:** + Demonstrates… more
- Merck (Boston, MA)
- …portfolio and compliance with public disclosure of clinical trials and their results. The Senior Informed Consent Medical Writer is responsible for ... regulatory requirements, and health literacy principles. With oversight, the Informed Consent Medical Writer: + Demonstrates growing independence managing… more
- Dana-Farber Cancer Institute (Brookline, MA)
- …Medicare Coverage Analyst (MCA) is responsible for reviewing clinical research protocols, Informed Consent Forms, Clinical Trial Agreements, and other relevant ... create a coverage analysis/billing guide. The coverage analysis indicates which medical procedures/services maybe 'Routine Cost' and billable to patient insurance… more
- Fenway Health (Boston, MA)
- …during clinical visits, in coordination with providers and research staff + Conducts informed consent and behavioral assessments in a respectful, affirming, and ... Senior Research Assistant, Data Studies Boston, MA (http://maps.google.com/maps?q=1340+Boylston+St+Boston+MA+USA+02215)...RA will lead recruitment and retention efforts in a medical setting, manage specimen processing (including PBMC isolation and… more
- Beth Israel Lahey Health (Boston, MA)
- …prior to entering the study and throughout the entire treatment. Discusses and obtains informed consent with patients. Revises protocol consent form to ... of the BDIMC Clinical Research Coordinator Core at Beth Israel Deaconess Medical Center (BIDMC). The Clinical Research Coordinator Core provides support for… more
- Dana-Farber Cancer Institute (Boston, MA)
- …protocols). This individual may also screen patients for protocol eligibility, obtain informed consent , and register study participants to clinical trials. Some ... in the clinical trial setting and identifying potential targets for intervention. The Senior CRC supports the research team in the overall conduct of clinical trials… more
- Sumitomo Pharma (Boston, MA)
- … safety subject matter expert (SME) on behalf of PVRM for: Study Protocols, Informed Consent Forms (ICF), Safety Management Plans (SMP), Clinical Study Reports ... signal evaluation reports according to established safety governance policies and keeping senior leadership informed of safety issues. **Job Duties and… more
- Dana-Farber Cancer Institute (Boston, MA)
- …Studies Program. This position may also screen patients for protocol eligibility, obtain informed consent , and register study participants to cohort and banking ... Medical School-affiliated hospitals. + Screen patients for protocol eligibility, obtain informed consent , and register study participants to cohort studies. +… more
- Pfizer (Boston, MA)
- …other clinical and medical colleagues, with authoring protocols, study level informed consent documents, site training materials, and other clinical and ... disease area(s) of assignment. + Support other clinical and medical colleagues, clinical operations and other functional lines for...of the drug, keeping the clinical and safety colleagues informed of changes in the safety profile as they… more