- Merck (Oklahoma City, OK)
- …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 (Oklahoma City, OK)
- …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 (Oklahoma City, OK)
- …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 (Oklahoma City, OK)
- … 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