- Merck (Sacramento, CA)
- …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 (Sacramento, CA)
- …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
- UCLA Health (Los Angeles, CA)
- …technique, alternatives, risks and problems, thus obtaining proper documented legal informed consent prior to the administration of anesthesia. Required: ... Description Under the supervision of an anesthesiologist, the Sr . Nurse Anesthetist will perform safe anesthesia care,...from anesthesia, transport of patient to recovery room and informed report to qualified medical personnel who… more
- Edwards Lifesciences (San Francisco, CA)
- …to develop process improvements. + Contribute to the development of clinical protocols, informed consent forms, and case report forms, and participate in team ... the trial/study. + Ensure source documentation is properly recorded and edit/amend informed consent documents as needed. + Perform other incidental duties… more
- Abbott (Santa Clara, CA)
- …clinical study reports, clinical study protocols, case report forms, investigational brochures, and informed consent forms. + Will assist in the development of ... spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues… more
- BeOne Medicines (San Mateo, CA)
- …and review of safety communication documents (eg, Dear Investigator Letter, Informed Consent Form, Investigator's Brochure, Healthcare Professional REV. 20 ... **_General Description:_** The Senior Manager, Safety Scientist supports assigned compounds in...Safety Analysis Plans (SAPs), Tables Figures and Listings (TFLs), Medical Monitoring Plans, CSRs (incl. China ADR Summary) and… more
- BeOne Medicines (San Mateo, CA)
- …but not limited to: + Protocol concepts, synopses, protocols, and amendments + Informed consent documents + Investigator Brochures + Clinical study reports + ... The Senior Director, Clinical Development, Solid Tumors will support...Development, Solid Tumors will support BeOne Medicine's Clinical and Medical assets by successful execution of clinical development programs… more
- Charles River Laboratories (Northridge, CA)
- …following: + Annual reporting for approved studies and study sites. + Protocol and informed consent revisions. + New study site submissions and approvals. + ... performing collections. The position works closely with QA management staff, the Medical Director, Operations Team, etc. to ensure all regulatory documents and… more
- Stanford Health Care (Palo Alto, CA)
- …to multi-task, prioritize effectively and attention to detail to avoid protocol deviations. + Informed Consent Process + Manages the consent process to ... sites staffed by Stanford's team of renowned surgical oncologists, medical oncologists, radiation oncologists and more enables care for...of any concerns raised by the patient during the informed consent process. + Assures that the… more
- Sumitomo Pharma (Sacramento, CA)
- … 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