- Merck (Washington, DC)
- …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 (Washington, DC)
- …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
- Johns Hopkins University (Columbia, MD)
- …for clinical research protocols in collaboration with other staff. Responsible to obtain informed consent from study participants. + Remain proficient in the ... and physical including chief compliant, presenting signs and symptoms, and past medical history and interval history. + Recognize differences between normal and… more
- Sumitomo Pharma (Washington, DC)
- … 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