- Merck (Dover, DE)
- …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 (Dover, DE)
- …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
- Sumitomo Pharma (Dover, DE)
- … 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
- University of Pennsylvania (Philadelphia, PA)
- …inpatient hospital setting; screen/enroll eligible subjects 5 days/week, in-person; obtain informed consent from study subjects or their proxies (in-person ... study enrollment packets. + Approach all eligible subjects every weekday and obtain informed consent . + Collection of multiple sets of human or environmental… more
- University of Pennsylvania (Philadelphia, PA)
- …support to Investigators and research staff in the development of research protocols, informed consent forms, case report forms, and other related study ... Pennsylvania. The Clinical Research Quality Specialist will work with senior team members to facilitate and conduct high quality...monitoring or auditing of studies + Development of protocols, consent forms, and case report forms + Coordination of… more