- Merck (Hartford, CT)
- …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 (Hartford, CT)
- …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
- Nuvance Health (Danbury, CT)
- …and testing to patients at risk for hereditary cancer. Assists them in making informed medical decisions based on their own personal risk assessment. * Develops ... *Description* * Senior Genetics Counselor - Danbury, CT* *Summary:* The...skills. * Understands legal implications of clinical procedures. Discusses informed consent including issues of privacy, confidentiality… more
- University of Connecticut Foundation Inc (Farmington, CT)
- …championships. UConn Health is a top-ranked health provider that delivers groundbreaking medical education, research, and hospital and clinical services to over one ... we strive for continued growth each and every day. POSITION SUMMARY The Senior Associate Vice President (SAVP) for Health Giving serves as the senior… more
- Sumitomo Pharma (Hartford, CT)
- … 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 (Groton, CT)
- …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 (Groton, CT)
- …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