- Lilly (Boston, MA)
- …+ Author, review and approve key documents, including protocols, risk profiles, informed consent documents, clinical study reports, and disclosure of research ... relevant protocol sections, and review and approve protocols + Contribute to informed consent documents, clinical study reports, publications, and other… 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
- 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 ... meetings as required or address IRB questions regarding the protocols or consent forms. Working with the principal investigator and/or research nurse, submits… 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
- Pfizer (Cambridge, 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
- Pfizer (Cambridge, MA)
- …integrity and quality of the clinical trial(s). + Authors protocols, study level informed consent documents, and contributes to authoring of IBs, site training ... area(s) of assignment. + Partners with 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
- Advocates (Framingham, MA)
- …philanthropic and other financial supports. + Ensure compliance with all documentation, informed consent , baseline and ongoing outcomes data collection at ... operational and financial targets. + Collaborate with executive and senior leaders across the agency to further develop and...Ability to use an Electronic Health Record to document medical necessary clinical services. + Must be able to… more