- Merck (Topeka, KS)
- …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 (Topeka, KS)
- …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
- Edwards Lifesciences (Topeka, KS)
- …developing process improvements. + Contribute to the development of clinical protocols, informed consent forms, and case report forms. Also contribute to ... conduct the trial/study, and source documentation is properly recorded. + Edit/amend informed consent documents. **What you'll need (Required):** + Bachelor's… more
- Sumitomo Pharma (Topeka, KS)
- … 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
- HCA Healthcare (Overland Park, KS)
- …physician and patient + Ensures the protection of study patients by verifying informed consent procedures and adhering to protocol requirements + Ensures the ... family! Jump-start your career as a Clinical Research Coordinator today with Menorah Medical Center. **Benefits** Menorah Medical Center, offers a total rewards… more